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...

Descripción completa

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

Internet

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

Ejemplares similares