Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy

PURPOSE: Congenital muscular dystrophy (CMD) comprises a rare group of genetic muscle diseases that present at birth or early during infancy. Two common subtypes of CMD are collagen VI-related muscular dystrophy (COL6-RD) and laminin alpha 2-related dystrophy (LAMA2-RD). Traditional outcome measures...

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Publicado no:Neuromuscul Disord
Main Authors: Bendixen, Roxanna M., Butrum, Jocelyn, Jain, Mina S., Parks, Rebecca, Hodsdon, Bonnie, Nichols, Carmel, Hsia, Michelle, Nelson, Leslie, Keller, Katherine C., McGuire, Michelle, Elliott, Jeffrey S., Linton, Melody M., Arveson, Irene C., Tounkara, Fatou, Vasavada, Ruhi, Harnett, Elizabeth, Punjabi, Monal, Donkervoort, Sandra, Dastgir, Jahannaz, Leach, Meganne E., Rutkowski, Anne, Waite, Melissa, Collins, James, Bönnemann, Carsten G., Meilleur, Katherine G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5318262/
https://ncbi.nlm.nih.gov/pubmed/28087121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2016.11.017
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