Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2261

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death ; volume:19 ; number:1 ; day:17 ; month:12 ; year:2019 ; pages:1-9 ; date:12.2019
BMC cardiovascular disorders ; 19, Heft 1 (17.12.2019), 1-9, 12.2019

Creator: Yokokawa, Tetsuro
Ichimura, Shohei
Hijioka, Naoko
Kaneshiro, Takashi
Yoshihisa, Akiomi
Kunii, Hiroyuki
Nakazato, Kazuhiko
Ishida, Takafumi
Suzuki, Osamu
Ohno, Seiko
Aiba, Takeshi
Ohtani, Hiroshi
Takeishi, Yasuchika

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12872-019-01282-6

URN: urn:nbn:de:101:1-2020040721584815946963

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:46 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Yokokawa, Tetsuro
Ichimura, Shohei
Hijioka, Naoko
Kaneshiro, Takashi
Yoshihisa, Akiomi
Kunii, Hiroyuki
Nakazato, Kazuhiko
Ishida, Takafumi
Suzuki, Osamu
Ohno, Seiko
Aiba, Takeshi
Ohtani, Hiroshi
Takeishi, Yasuchika
SpringerLink (Online service)

Other Objects (12)

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Cardiomyopathy, familial dilated

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy

Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

Sudden Cardiac Death Prediction in Non-ischemic Dilated Cardiomyopathy: a Multiparametric and Dynamic Approach

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report

Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity

Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Dilated cardiomyopathies and non-compaction cardiomyopathy

Related objects

Reset password