The Proteomic Profile of Hereditary Inclusion Body Myopathy

Author:

Sela Ilan,Milman Krentsis Irit,Shlomai Zipora,Sadeh Menachem,Dabby Ron,Argov Zohar,Ben-Bassat Hannah,Mitrani-Rosenbaum Stella

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference39 articles.

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2. Newest approaches to diagnosis of sporadic inclusion body myositis and hereditary inclusion body myopathies, including molecular-pathologic similarities to Alzheimer disease.;V Askanas,1998

3. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.;I Eisenberg;Nat Genet,2001

4. Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy.;I Nonaka;Curr Neurol Neurosci Rep,2005

5. Mutation spectrum of the GNE gene in hereditary inclusion body myopathy sparing the quadriceps.;I Eisenberg;Hum Mutat,2003

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