Article

Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy

2022-06-27

Abstract excerpt

<h4>Background: </h4> Familial dilated cardiomyopathy (DCM) is a genetic cardiomyopathy that is associated with reduced left ventricle function or systolic function. Fifty-one DCM-causative genes have been reported, most of which are inherited in an autosomal dominant manner. However, recessive DCM-causative gene is rarely observed. <h4>Methods: </h4> Whole-exome sequencing (WES) was performed in a consanguineous...

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Literature Corpus work: 74a0cdc1-9580-5d0f-8f1c-16cda673f84d
DOI: 10.21203/rs.3.rs-1693689/v1

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