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	Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report
	Zhao, Xiangzhong; Lu, Jingru; Gao, Yanxia; Wang, Xiaoling; Lang, Yanhua; Shao, Leping
刊名	BMC NEPHROLOGY
	2018
卷号	19期号:1
关键词	Distal renal tubular acidosis ATP6V1B1 gene Sensorineural hearing loss Enlarged vestibular aqueduct
DOI	10.1186/s12882-018-1173-1
URL标识	查看原文
公开日期	[db:dc_date_available]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4571149
专题	山东大学
作者单位	Qingdao Univ, Affiliated Hosp, Cent Lab, 1677 Wutaishan Rd, Qingdao 266555,
推荐引用方式 GB/T 7714	Zhao, Xiangzhong,Lu, Jingru,Gao, Yanxia,et al. Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report[J]. BMC NEPHROLOGY,2018,19(1).
APA	Zhao, Xiangzhong,Lu, Jingru,Gao, Yanxia,Wang, Xiaoling,Lang, Yanhua,&Shao, Leping.(2018).Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report.BMC NEPHROLOGY,19(1).
MLA	Zhao, Xiangzhong,et al."Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report".BMC NEPHROLOGY 19.1(2018).

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