Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation

Author:

Guo Fengfeng,Sun Yaxun,Wang Hongkun,Wang Hao,Zhou Jingjun,Fan Hangping,Su Jun,Gong Tingyu,Jiang Chenyang,Liang Ping

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference5 articles.

1. Prevalence of the congenital long-QT syndrome;Schwartz;Circulation,2009

2. Impact of genetics on the clinical management of channelopathies;Schwartz;J. Am. Coll. Cardiol.,2013

3. Genetic and clinical advances in congenital long QT syndrome;Mizusawa;Circ. J.,2014

4. Long-QT syndrome: from genetics to management;Schwartz;Circ. Arrhythm. Electrophysiol.,2012

5. Generation of five induced pluripotent stem cell lines with DMD/c.497G > T mutation from renal epithelial cells of a Duchenne muscular dystrophy patient and a recessive carrier parent;Su;Stem Cell Res,2020

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