Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death-Reference-Cited by-同舟云学术

Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death

Published:2018-03 Issue:2 Volume:51 Page:309-315
ISSN:0022-0736
Container-title:Journal of Electrocardiology
language:en
Short-container-title:Journal of Electrocardiology

Author:

Lin Yubi,He Siqi,Liao Zili,Feng Ruiling,Liu Ruilin,Peng Yongzheng,Yu Nan,Qi Hang,Chen Jia,Huang Zifeng,Lei Heping,Liu Yang,Rao Fang,Deng Chunyu,Xue Yumei,Zhang Guolin,Zhang Bin,Yao Hua,Wu Shulin

Funder

Science and Technology Program of Guangdong Province

Science and Technology Program of Guangzhou City

Science and Technology Innovation Project of Guangzhou City

Natural Science Foundation of Guangdong Province

Science and Technology Development of Special Funding of Guangdong Province

Livelihood Science and Technology Topics of Major Projects of Industrial-University Collaborative Innovation

Science and Technology Planning Project of Guangdong Province

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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