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	A novel phenotype with splicing mutation identified in a Chinese family with desminopathy
	Fan, Peng; Lu, Chao-Xia; Dong, Xue-Qi; Zhu, Di; Yang, Kun-Qi; Liu, Ke-Qiang; Zhang, Di; Zhang, Ying; Meng, Xu; Tan, Hui-Qiong
	2019
卷号	132期号:2页码:127-134
关键词	Desminopathy Cardiomyopathy Desmin gene Splicing mutation
ISSN号	0366-6999
DOI	10.1097/CM9.0000000000000001
URL标识	查看原文
收录类别	SCIE ; PUBMED ; CSCD ; CMA系列
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6345545
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	Fan, Peng,Lu, Chao-Xia,Dong, Xue-Qi,et al. A novel phenotype with splicing mutation identified in a Chinese family with desminopathy[J],2019,132(2):127-134.
APA	Fan, Peng.,Lu, Chao-Xia.,Dong, Xue-Qi.,Zhu, Di.,Yang, Kun-Qi.,...&Zhou, Xian-Liang.(2019).A novel phenotype with splicing mutation identified in a Chinese family with desminopathy.,132(2),127-134.
MLA	Fan, Peng,et al."A novel phenotype with splicing mutation identified in a Chinese family with desminopathy".132.2(2019):127-134.

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