A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome

An autosomal recessive neuromuscular disorder characterized by skeletal muscle weakness, fatigability and variable electromyographic or muscular histopathological features has been described in the two related Sphynx and Devon Rex cat breeds (Felis catus). Collection of data from two affected Sphynx...

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Publicado en:PLoS One
Autores principales: Abitbol, Marie, Hitte, Christophe, Bossé, Philippe, Blanchard-Gutton, Nicolas, Thomas, Anne, Martignat, Lionel, Blot, Stéphane, Tiret, Laurent
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4556666/
https://ncbi.nlm.nih.gov/pubmed/26327126
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0137019
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