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	A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia
	Fu Rong; Lu Lin; Jiang Jun; Nie Min; Wang Xiaojing; Lu Zhaolin
	2017
卷号	96期号:21页码:e6994
关键词	congenital adrenal hyperplasia lipoid congenital adrenal hyperplasia STAR mutation
ISSN号	0025-7974
DOI	10.1097/MD.0000000000006994
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/6368163
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	Fu Rong,Lu Lin,Jiang Jun,et al. A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia[J],2017,96(21):e6994.
APA	Fu Rong,Lu Lin,Jiang Jun,Nie Min,Wang Xiaojing,&Lu Zhaolin.(2017).A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia.,96(21),e6994.
MLA	Fu Rong,et al."A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia".96.21(2017):e6994.

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