Articles with "dystrophy activating" as a keyword



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Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle.

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Published in 2018 at "Human molecular genetics"

DOI: 10.1093/hmg/ddy162

Abstract: Facioscapulohumeral dystrophy (FSHD) is the third most prevalent muscular dystrophy. A progressive disease, it presents clinically as weakness and wasting of the face, shoulder and upper arm muscles, with later involvement of the trunk and… read more here.

Keywords: skeletal muscle; muscle; dystrophy; dystrophy activating ... See more keywords