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Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern

BACKGROUND: Limb girdle muscular dystrophy type 2G (LGMD2G) is a subtype of autosomal recessive muscular dystrophy caused by mutations in the telethonin gene. There are few LGMD2G patients worldwide reported, and this is the first description associated with early tibialis anterior sparing on muscle...

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Detalhes bibliográficos
Main Authors: Cotta, Ana, Paim, Julia Filardi, da-Cunha-Junior, Antonio Lopes, Neto, Rafael Xavier, Nunes, Simone Vilela, Navarro, Monica Magalhaes, Valicek, Jaquelin, Carvalho, Elmano, Yamamoto, Lydia U, Almeida, Camila F, Braz, Shelida Vasconcelos, Takata, Reinaldo Issao, Vainzof, Mariz
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4188961/
https://ncbi.nlm.nih.gov/pubmed/25298746
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6890-14-41
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