The Proteomic Profile of Hereditary Inclusion Body Myopathy

Hereditary inclusion body myopathy (HIBM) is an adult onset, slowly progressive distal and proximal myopathy. Although the causing gene, GNE, encodes for a key enzyme in the biosynthesis of sialic acid, its primary function in HIBM remains unknown. The goal of this study was to unravel new clues on...

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Detalles Bibliográficos
Autores principales: Sela, Ilan, Milman Krentsis, Irit, Shlomai, Zipora, Sadeh, Menachem, Dabby, Ron, Argov, Zohar, Ben-Bassat, Hannah, Mitrani-Rosenbaum, Stella
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031555/
https://www.ncbi.nlm.nih.gov/pubmed/21305017
http://dx.doi.org/10.1371/journal.pone.0016334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031555/
https://www.ncbi.nlm.nih.gov/pubmed/21305017
http://dx.doi.org/10.1371/journal.pone.0016334

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