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	Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I-Na contributing to LQT syndrome
	Hu, Rou-Mu; Tan, Bi-Hua; Orland, Kate M.; Valdivia, Carmen R.; Peterson, Amber; Pu, Jielin; Makielski, Jonathan C.
	2013
卷号	304期号:7页码:H994-H1001
关键词	long QT syndrome SCN5a alpha(1)-syntrophin late sodium current
ISSN号	0363-6135
DOI	10.1152/ajpheart.00705.2012
URL标识	查看原文
收录类别	SCIE ; PUBMED
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6704318
专题	中国医学科学院 北京协和医学院
推荐引用方式 GB/T 7714	Hu, Rou-Mu,Tan, Bi-Hua,Orland, Kate M.,et al. Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I-Na contributing to LQT syndrome[J],2013,304(7):H994-H1001.
APA	Hu, Rou-Mu.,Tan, Bi-Hua.,Orland, Kate M..,Valdivia, Carmen R..,Peterson, Amber.,...&Makielski, Jonathan C..(2013).Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I-Na contributing to LQT syndrome.,304(7),H994-H1001.
MLA	Hu, Rou-Mu,et al."Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I-Na contributing to LQT syndrome".304.7(2013):H994-H1001.

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