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Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy

发布时间：2019-10-25

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发表刊物：Cardiology

论文类型：基础研究

卷号：136

期号：1

页面范围：10-14

是否译文：否

上一条： Whole exome sequencing identified a novel mutation (p. Ala1884Pro) of β‐spectrin in a Chinese family with hereditary spherocytosis

下一条： Whole Exome Sequencing identifies a Novel Mutation (p.L320R) of Actinin Alpha 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia