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	SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency
	Zeng, Han-Shi[1]; Lin, Wei-Xia[1]; Zhao, Shu-Tao[1]; Zhang, Zhan-Hui[2]; Yang, Heng-Wen[3]; Chen, Feng-Ping[4]; Song, Yuan-Zong[1]; Yin, Zhi-Nan[3]
	2016
卷号	14期号:6页码:5189
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4306850
专题	暨南大学
作者单位	1.[1]Jinan Univ, Affiliated Hosp 1, Dept Pediat, 613 Huangpu Da Dao Xi, Guangzhou 510630, Guangdong, Peoples R China 2.[2]Jinan Univ, Affiliated Hosp 1, Core Lab, Guangzhou 510630, Guangdong, Peoples R China 3.[3]Jinan Univ, Affiliated Hosp 1, Biomed Translat Res Inst, Guangzhou 510630, Guangdong, Peoples R China 4.[4]Jinan Univ, Affiliated Hosp 1, Dept Lab Sci, Guangzhou 510630, Guangdong, Peoples R China
推荐引用方式 GB/T 7714	Zeng, Han-Shi[1],Lin, Wei-Xia[1],Zhao, Shu-Tao[1],et al. SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency[J],2016,14(6):5189.
APA	Zeng, Han-Shi[1].,Lin, Wei-Xia[1].,Zhao, Shu-Tao[1].,Zhang, Zhan-Hui[2].,Yang, Heng-Wen[3].,...&Yin, Zhi-Nan[3].(2016).SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency.,14(6),5189.
MLA	Zeng, Han-Shi[1],et al."SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency".14.6(2016):5189.

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