Whole-exome sequencing identifies a novel mutation of...

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Journal of Cellular and Molecular Medicine 2017 / 10

Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death

Huang, Hao, Chen, Ya-Qin, Fan, Liang-Liang, Guo, Shuai, Li, Jing-Jing, Jin, Jie-Yuan, Xiang, Rong
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Language:
english
Journal:
Journal of Cellular and Molecular Medicine
DOI:
10.1111/jcmm.13409
Date:
October, 2017
File:
PDF, 424 KB
english, 2017
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