关键词: DUX4 Epigenetic Facioscapulohumeral muscular dystrophy Hypomethylation Muscle pathology SMCHD1
Mesh : Adult Child, Preschool Genetic Testing / methods Homeodomain Proteins / genetics Humans Male Middle Aged Muscular Dystrophy, Facioscapulohumeral / diagnosis genetics Phenotype
来 源:
DOI:10.1016/j.ncl.2020.03.003
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