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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Hlavní autoři: Sancisi, Valentina, Germinario, Elena, Esposito, Alessandra, Morini, Elisabetta, Peron, Samantha, Moggio, Maurizio, Tomelleri, Giuliano, Danieli-Betto, Daniela, Tupler, Rossella
Médium: Artigo
Jazyk:Inglês
Vydáno: American Physiological Society 2013
Témata:
Translational Physiology
On-line přístup: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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