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Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian family

INTRODUCTION: Dilated cardiomyopathy (DCM) is characterized by the dilation and impaired contraction of 1 or both ventricles and can be caused by a variety of disorders. Up to 50% of idiopathic DCM cases have heritable familial diseases, and the clinical screening of family members is recommended. I...

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Detalles Bibliográficos
Autores principales:	Malakootian, Mahshid, Bagheri Moghaddam, Mahrokh, Kalayinia, Samira, Farrashi, Melody, Maleki, Majid, Sadeghipour, Parham, Amin, Ahmad
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079971/ https://www.ncbi.nlm.nih.gov/pubmed/35527250 http://dx.doi.org/10.1186/s12920-022-01262-4

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