Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation
OBJECTIVE: This study aimed to identify novel GATA5 mutations that underlie familial atrial fibrillation. METHODS: A total of 110 unrelated patients with familial atrial fibrillation and 200 unrelated, ethnically matched healthy controls were recruited. The entire coding region of the GATA5 gene was...
Main Authors: | Jian-Yun Gu, Jia-Hong Xu, Hong Yu, Yi-Qing Yang |
---|---|
Format: | Article |
Language: | English |
Published: |
Faculdade de Medicina / USP
2012-12-01
|
Series: | Clinics |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322012001200008 |
Similar Items
-
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation
by: Xing-Biao Qiu, et al.
Published: (2014-01-01) -
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation
by: Wen-Hui Xie, et al.
Published: (2013-06-01) -
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy
by: Ning Li, et al.
Published: (2021-03-01) -
Genetic varients leading to atrial fibrillation
by: Abraham, Elizabeth June
Published: (2016) -
Gata6 Haploinsufficiency Leads to Aortic Valve, Conduction System and Limbs Defects
by: Gharibeh, Lara
Published: (2018)