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	Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome
	Liu, Jia-Wei; Si, Nuo; Wang, Lian-Qing; Shen, Ti; Zeng, Xue-Jun; Zhang, Xue; Ma, Dong-Lai
	2015
卷号	128期号:10页码:1336-1339
关键词	China H syndrome Novel Mutation The Solute Carrier Family 29 Member 3 Gene
ISSN号	0366-6999
DOI	10.4103/0366-6999.156778
URL标识	查看原文
收录类别	SCIE ; PUBMED ; ISTIC ; CSCD ; CMA系列
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6662352
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	Liu, Jia-Wei,Si, Nuo,Wang, Lian-Qing,et al. Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome[J],2015,128(10):1336-1339.
APA	Liu, Jia-Wei.,Si, Nuo.,Wang, Lian-Qing.,Shen, Ti.,Zeng, Xue-Jun.,...&Ma, Dong-Lai.(2015).Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome.,128(10),1336-1339.
MLA	Liu, Jia-Wei,et al."Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome".128.10(2015):1336-1339.

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