A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing

BACKGROUND: Familial dilated cardiomyopathy (DCM) is a genetic heart disorder characterized by progressive heart failure and sudden cardiac death. Over 250 genes have been reported in association with DCM; nonetheless, the genetic cause of most DCM patients has been unknown. The goal of the present...

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Detalles Bibliográficos
Autores principales: Ghasemi, Serwa, Mahdavi, Mohammad, Maleki, Majid, Salahshourifar, Iman, Kalayinia, Samira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641816/
https://www.ncbi.nlm.nih.gov/pubmed/36344977
http://dx.doi.org/10.1186/s12920-022-01388-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641816/
https://www.ncbi.nlm.nih.gov/pubmed/36344977
http://dx.doi.org/10.1186/s12920-022-01388-5

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