FHL1 Reduces Dystrophy in Transgenic Mice Overexpressing FSHD Muscular Dystrophy Region Gene 1 (FRG1)

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant disease with no effective treatment. The genetic cause of FSHD is complex and the primary pathogenic insult underlying the muscle disease is unknown. Several disease candidate genes have been proposed including DUX4 and FRG1. Exp...

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Detalles Bibliográficos
Autores principales: Feeney, Sandra J., McGrath, Meagan J., Sriratana, Absorn, Gehrig, Stefan M., Lynch, Gordon S., D’Arcy, Colleen E., Price, John T., McLean, Catriona A., Tupler, Rossella, Mitchell, Christina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335040/
https://www.ncbi.nlm.nih.gov/pubmed/25695429
http://dx.doi.org/10.1371/journal.pone.0117665

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335040/
https://www.ncbi.nlm.nih.gov/pubmed/25695429
http://dx.doi.org/10.1371/journal.pone.0117665

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