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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| Main Authors: | , , , , , , |
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| Format: | Book |
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BMC,
2022-05-01T00:00:00Z.
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