Meeting report: the 2021 FSHD International Research Congress
Meeting report: the 2021 FSHD International Research Congress
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Facioscapulohumeral muscular dystrophy (FSHD) is the second most common genetic myopathy, characterized by slowly progressing and highly heterogeneous muscle wasting with a typical onset in the late teens/early adulthood [1]. Although the etiology of the disease for both FSHD type 1 and type 2 has been attributed to gain-of-toxic function stemming...
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Meeting report: the 2021 FSHD International Research Congress
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TN_cdi_doaj_primary_oai_doaj_org_article_e1293d0484d644569819137cb3f35b3b
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e1293d0484d644569819137cb3f35b3b
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ISSN
2044-5040
E-ISSN
2044-5040
DOI
10.1186/s13395-022-00287-8
