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

BACKGROUND: 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...

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Detalles Bibliográficos
Autores principales: Luo, Kai, Zheng, Chenqing, Luo, Rong, Cao, Xin, Sun, Huajun, Ma, Huihui, Huang, Jichang, Yang, Xu, Wu, Xiushan, Li, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446846/
https://www.ncbi.nlm.nih.gov/pubmed/36068540
http://dx.doi.org/10.1186/s12920-022-01349-y

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