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	Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
	Wang, Rongrong; Yang, Shuanghao; Xu, Ming; Huang, Jia; Liu, Hongyan; Gu, Weiyue; Zhang, Xue
	2018
卷号	61期号:8页码:947-953
关键词	hereditary spherocytosis mutation ANK1 SPTB SLC4A1 whole-exome sequencing
ISSN号	1674-7305
DOI	10.1007/s11427-017-9232-6
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/6360132
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	Wang, Rongrong,Yang, Shuanghao,Xu, Ming,et al. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis[J],2018,61(8):947-953.
APA	Wang, Rongrong.,Yang, Shuanghao.,Xu, Ming.,Huang, Jia.,Liu, Hongyan.,...&Zhang, Xue.(2018).Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis.,61(8),947-953.
MLA	Wang, Rongrong,et al."Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis".61.8(2018):947-953.

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