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

Abstract 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 recomm...

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Autors principals: Mahshid Malakootian (Autor), Mahrokh Bagheri Moghaddam (Autor), Samira Kalayinia (Autor), Melody Farrashi (Autor), Majid Maleki (Autor), Parham Sadeghipour (Autor), Ahmad Amin (Autor)
Format: Llibre
Publicat: BMC, 2022-05-01T00:00:00Z.
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