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

• Auteurs principaux: Serwa Ghasemi (Auteur), Mohammad Mahdavi (Auteur), Majid Maleki (Auteur), Iman Salahshourifar (Auteur), Samira Kalayinia (Auteur)
• Format: Livre
• Publié: BMC, 2022-11-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Abstract 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...