PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

OBJECTIVE: This study aimed to identify novel PITX2c mutations responsible for idiopathic atrial fibrillation. METHODS: A cohort of 210 unrelated patients with idiopathic atrial fibrillation and 200 unrelated, ethnically matched healthy individuals used as controls were recruited. The whole coding e...

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Detalles Bibliográficos
Autores principales: Qiu, Xing-Biao, Xu, Ying-Jia, Li, Ruo-Gu, Xu, Lei, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Qu, Xin-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2014
Materias:
Clinical Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870307/
https://www.ncbi.nlm.nih.gov/pubmed/24473555
http://dx.doi.org/10.6061/clinics/2014(01)03

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870307/
https://www.ncbi.nlm.nih.gov/pubmed/24473555
http://dx.doi.org/10.6061/clinics/2014(01)03

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