Novel Pathogenic Variants in a French Cohort Widen the Mutational Spectrum of GNE Myopathy

Background: GNE myopathy is a rare autosomal recessively inherited muscle disease resulting from mutations in the gene encoding GNE (UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase), a key enzyme in sialic acid biosynthesis. 154 different pathogenic variants have been previously assoc...

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Detalles Bibliográficos
Autores principales: Cerino, Mathieu, Gorokhova, Svetlana, Béhin, Anthony, Urtizberea, Jon Andoni, Kergourlay, Virginie, Salvo, Eric, Bernard, Rafaëlle, Lévy, Nicolas, Bartoli, Marc, Krahn, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2015
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278624/
https://www.ncbi.nlm.nih.gov/pubmed/27858732
http://dx.doi.org/10.3233/JND-150074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278624/
https://www.ncbi.nlm.nih.gov/pubmed/27858732
http://dx.doi.org/10.3233/JND-150074

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