Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)

Facioscapulohumeral muscular dystrophy (FSHD), a common hereditary myopathy, is characterized by atrophy and weakness of selective muscle groups. FSHD is considered an autosomal dominant disease with incomplete penetrance and unpredictable variability of clinical expression within families. Mice ove...

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Autori principali: Sancisi, Valentina, Germinario, Elena, Esposito, Alessandra, Morini, Elisabetta, Peron, Samantha, Moggio, Maurizio, Tomelleri, Giuliano, Danieli-Betto, Daniela, Tupler, Rossella
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Physiological Society 2013
Soggetti:
Translational Physiology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3921317/
https://ncbi.nlm.nih.gov/pubmed/24305066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpregu.00379.2013
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