Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation-Reference-Cited by-同舟云学术

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation

Published:2019-11 Issue: Volume:43 Page:102159
ISSN:1872-4973
Container-title:Forensic Science International: Genetics
language:en
Short-container-title:Forensic Science International: Genetics

Author:

Santori Montserrat,Gil Rocío,Blanco-Verea Alejandro,Riuró Helena,Díaz-Castro Óscar,López-Abel Bernardo,Brugada Ramón,Carracedo Ángel,Pérez Guillermo J.,Scornik Fabiana S.,Brion María

Funder

Instituto de Salud Carlos III

Fondo Europeo de Desarrollo Regional

Fundación Salud 2000

Publisher

Elsevier BV

Subject

Genetics,Pathology and Forensic Medicine

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4. Cardiac ion channelopathies and the sudden infant death syndrome;Wilders;ISRN Cardiol.,2012

5. HERG, a human inward rectifier in the voltage-gated potassium channel family;Trudeau;Science,1995

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