- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Missense mutations in the CITED2 gene may contribute to congenital heart disease ; volume:24 ; number:1 ; day:27 ; month:9 ; year:2024 ; pages:1-10 ; date:12.2024
BMC cardiovascular disorders ; 24, Heft 1 (27.9.2024), 1-10, 12.2024
- Creator
-
Yaqoob, Hira
Ahmad, Hussain
Ali, Syed Irtiza
Patel, Najma
Arif, Afsheen
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12872-024-04035-2
- URN
-
urn:nbn:de:101:1-2412132100473.575695812465
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Yaqoob, Hira
- Ahmad, Hussain
- Ali, Syed Irtiza
- Patel, Najma
- Arif, Afsheen
- SpringerLink (Online service)
Other Objects (12)
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders
Endothelial microparticles are increased in congenital heart diseases and contribute to endothelial dysfunction
Functional analysis of disease-associated CASK missense mutations
Protein destabilization underlies pathogenic missense mutations in ARID1B
Role of SMAD4 missense mutations in colorectal cancer progression
Making sense of missense variants in TTN-related congenital myopathies
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders
Endothelial microparticles are increased in congenital heart diseases and contribute to endothelial dysfunction
Functional analysis of disease-associated CASK missense mutations
Protein destabilization underlies pathogenic missense mutations in ARID1B
Role of SMAD4 missense mutations in colorectal cancer progression
Making sense of missense variants in TTN-related congenital myopathies
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders
Endothelial microparticles are increased in congenital heart diseases and contribute to endothelial dysfunction
Functional analysis of disease-associated CASK missense mutations
Protein destabilization underlies pathogenic missense mutations in ARID1B
Role of SMAD4 missense mutations in colorectal cancer progression