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Published in 2022 at "Physiological Reports"
DOI: 10.14814/phy2.15277
Abstract: Facioscapulohumeral muscular dystrophy (FSHD), a common form of muscular dystrophy, is caused by a genetic mutation that alters DUX4 gene expression. This mutation contributes to significant skeletal muscle loss. Although it is suggested that cardiac…
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Keywords:
facioscapulohumeral muscular;
people fshd;
fshd controls;
muscular dystrophy ... See more keywords