Csrp3 (cysteine and glycine-rich protein 3)

基因基本信息

Csrp3 基因表型（MGI）

Homozygotes for a targeted null mutation exhibit dilated cardiomyopathy characterized by disrupted cardiomyocyte organization that results in premature death, left ventricle dilation, hypertrophy, decreased contractility, and fibrosis. Some homozygotes die postnataly due to heart failure.

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