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	Sodium taurocholate cotransporting polypeptide (NTCP) deficiency: Identification of a novel SLC10A1 mutation in two unrelated infants presenting with neonatal indirect hyperbilirubinemia and remarkable hypercholanemia
	Qiu, Jian-Wu[1]; Deng, Mei[1]; Cheng, Ying[1]; Atif, Raza-Muhammad[1]; Lin, Wei-Xia[1]; Guo, Li[1]; Li, Hua[1]; Song, Yuan-Zong[1]
	2017
卷号	8期号:63页码:106598
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/4444634
专题	暨南大学
作者单位	[1]Jinan Univ, Affiliated Hosp 1, Dept Pediat, Guangzhou 510630, Guangdong, Peoples R China
推荐引用方式 GB/T 7714	Qiu, Jian-Wu[1],Deng, Mei[1],Cheng, Ying[1],et al. Sodium taurocholate cotransporting polypeptide (NTCP) deficiency: Identification of a novel SLC10A1 mutation in two unrelated infants presenting with neonatal indirect hyperbilirubinemia and remarkable hypercholanemia[J],2017,8(63):106598.
APA	Qiu, Jian-Wu[1].,Deng, Mei[1].,Cheng, Ying[1].,Atif, Raza-Muhammad[1].,Lin, Wei-Xia[1].,...&Song, Yuan-Zong[1].(2017).Sodium taurocholate cotransporting polypeptide (NTCP) deficiency: Identification of a novel SLC10A1 mutation in two unrelated infants presenting with neonatal indirect hyperbilirubinemia and remarkable hypercholanemia.,8(63),106598.
MLA	Qiu, Jian-Wu[1],et al."Sodium taurocholate cotransporting polypeptide (NTCP) deficiency: Identification of a novel SLC10A1 mutation in two unrelated infants presenting with neonatal indirect hyperbilirubinemia and remarkable hypercholanemia".8.63(2017):106598.

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