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Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy

BACKGROUND: Dilated cardiomyopathy (DCM), which is a major cause of heart failure, is a primary cardiac muscle disease with high morbidity and mortality rates. DCM is a genetically heritable disease and more than 10 gene ontologies have been implicated in DCM. CDH2 encodes N-cadherin and belongs to...

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Detalles Bibliográficos
Autores principales: Chen, Yuanying, Sun, Qiqing, Hao, Chanjuan, Guo, Ruolan, Wang, Chentong, Yang, Weili, Zhang, Yaodong, Wang, Fangjie, Li, Wei, Guo, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468813/
https://www.ncbi.nlm.nih.gov/pubmed/36111109
http://dx.doi.org/10.3389/fmed.2022.944950