Associated Papers
A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation.
Ding DB et al.
Qjm : Monthly Journal of the Association of Physicians, 2018
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
Huang H et al.
Journal of Cellular and Molecular Medicine, 2018
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