Familial dilated cardiomyopathy caused by a novel variant in the Lamin A/C gene: a case report

BACKGROUND: Familial dilated cardiomyopathy (FDCM) is most commonly inherited as an autosomal dominant trait. The Lamin A/C (LMNA) gene variants have been identified to be associated with DCM, conductive system disorders, type 2 Emery-Dreifuss muscular dystrophy and several other disorders. Here, we...

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Detalles Bibliográficos
Autores principales: Huang, Jing, Wan, Qing, Zou, Yu, Wang, Lijie, Pan, Yesheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509919/
https://www.ncbi.nlm.nih.gov/pubmed/32962641
http://dx.doi.org/10.1186/s12872-020-01695-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509919/
https://www.ncbi.nlm.nih.gov/pubmed/32962641
http://dx.doi.org/10.1186/s12872-020-01695-8

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