A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy

Hereditary inclusion body myopathy (hIBM) is an adult-onset hereditary myopathy, usually with distal onset and quadriceps sparing. This myopathy is autosomal recessive and associated to UPD-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE) gene mutations. In this study, we report a no...

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Detalles Bibliográficos
Autores principales: Behnam, Mahdiyeh, Jin-Hong, Shin, Kim, Dae-Seong, Basiri, Keivan, Nilipour, Yalda, Sedghi, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235102/
https://www.ncbi.nlm.nih.gov/pubmed/25422667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235102/
https://www.ncbi.nlm.nih.gov/pubmed/25422667

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