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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Sela, Ilan, Milman Krentsis, Irit, Shlomai, Zipora, Sadeh, Menachem, Dabby, Ron, Argov, Zohar, Ben-Bassat, Hannah, Mitrani-Rosenbaum, Stella
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2011
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3031555/
https://ncbi.nlm.nih.gov/pubmed/21305017
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0016334
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