The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1326

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease ; volume:10 ; number:1 ; day:24 ; month:9 ; year:2015 ; pages:1-8 ; date:12.2015
Molecular neurodegeneration ; 10, Heft 1 (24.9.2015), 1-8, 12.2015

Creator: Mata, Ignacio F.
Jang, Yongwoo
Kim, Chun-Hyung
Hanna, David S.
Dorschner, Michael O.
Samii, Ali
Agarwal, Pinky
Roberts, John W.
Klepitskaya, Olga
Shprecher, David R.
Chung, Kathryn A.
Factor, Stewart A.
Espay, Alberto J.
Revilla, Fredy J.
Higgins, Donald S.
Litvan, Irene
Leverenz, James B.
Yearout, Dora
Inca-Martinez, Miguel
Martinez, Erica
Thompson, Tiffany R.
Cholerton, Brenna A.
Hu, Shu-Ching
Edwards, Karen L.
Kim, Kwang-Soo
Zabetian, Cyrus P.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13024-015-0045-4

URN: urn:nbn:de:101:1-2019120119205898929194

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

Last update: 14.08.2025, 10:56 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

Mata, Ignacio F.
Jang, Yongwoo
Kim, Chun-Hyung
Hanna, David S.
Dorschner, Michael O.
Samii, Ali
Agarwal, Pinky
Roberts, John W.
Klepitskaya, Olga
Shprecher, David R.
Chung, Kathryn A.
Factor, Stewart A.
Espay, Alberto J.
Revilla, Fredy J.
Higgins, Donald S.
Litvan, Irene
Leverenz, James B.
Yearout, Dora
Inca-Martinez, Miguel
Martinez, Erica
Thompson, Tiffany R.
Cholerton, Brenna A.
Hu, Shu-Ching
Edwards, Karen L.
Kim, Kwang-Soo
Zabetian, Cyrus P.
SpringerLink (Online service)

Other Objects (12)

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Hochschulschrift

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Hochschulschrift

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Hochschulschrift

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

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.

The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

X-linked SCID with a rare mutation

Novel gene (TMEM230) linked to Parkinson’s disease

Role of RNF113A in ribosomal performance and X-linked dominant trichothiodystrophy

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRKN-linked familial Parkinson’s disease: cellular and molecular mechanisms of disease-linked variants

Mutationen der Gene LRRK2 und SNCA bei autosomal-dominantem Parkinson-Syndrom in der Türkei

Parkinson’s disease is associated with clonal hematopoiesis with TET2 mutation

Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules

Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons

Easily misdiagnosed X-linked adrenoleukodystrophy

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

Related objects

Reset password