A Novel Bi-allelic Loss-of-Function Variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1 related myopathy.

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PMID: 31260566 [PubMed - as supplied by publisher]

Source: Clinical Genetics - June 30, 2019 Category: Genetics & Stem Cells Authors: Shukla A, Narayanan DL, Asher U, Girisha KM Tags: Clin Genet Source Type: research