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	Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death
	Lin, Yubi[1,2,3,4,5,6]; Liao, Zili[1,2,3,4,5]; He, Siqi[1,2,3,4,5,6]; Liu, Ruilin[7]; Peng, Yongzheng[8]; Yu, Nan[8]; Qi, Hang[8]; Chen, Jia[9]; Feng, Ruiling[1,2,3,4,5,6]; Huang, Zifeng[1,2,3,4,5,6]
会议日期	OCT 12-15, 2017
会议地点	Beijing, PEOPLES R CHINA
URL标识	查看原文
内容类型	会议论文
URI标识	http://www.corc.org.cn/handle/1471x/4629878
专题	暨南大学
作者单位	1.[1]South China Univ Technol, Guangdong Gen Hosp, Guangzhou, Guangdong, Peoples R China 2.[2]South China Univ Technol, Clin Coll 1, Med Sch, Guangzhou, Guangdong, Peoples R China 3.[3]Guangdong Cardiovasc Inst, Guangzhou, Guangdong, Peoples R China 4.[4]Guangdong Prov Key Lab South China Struct Heart D, Guangzhou, Guangdong, Peoples R China 5.[5]Guangdong Acad Med Sci, Guangzhou, Guangdong, Peoples R China 6.[6]Jinan Univ, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China 7.[7]Southern Med Univ, Shunde Hosp, Shunde, Peoples R China 8.[8]Southern Med Univ, Dept Clin Lab, Zhujiang Hosp, Guangzhou, Guangdong, Peoples R China 9.[9]Guangdong 2 Prov Peoples Hosp, Dept Cardiol 2, Guangzhou, Guangdong, Peoples R China 10.[10]Guangzhou Med Univ, Lin Hes Academician Workstn New Med & Clin Transl, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
推荐引用方式 GB/T 7714	Lin, Yubi[1,2,3,4,5,6],Liao, Zili[1,2,3,4,5],He, Siqi[1,2,3,4,5,6],et al. Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death[C]. 见:. Beijing, PEOPLES R CHINA. OCT 12-15, 2017.

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