Mitochondrial processes are impaired in hereditary inclusion body myopathy

By Eisenberg Iris   Novershtern Noa   Itzhaki Zohar   Becker-Cohen Michal   Sadeh Menachem   Willems Peter H.G.M.   Friedman Nir   Koopman Werner J.H.   Mitrani-Rosenbaum Stella  

Human Molecular Genetics, Vol. 17, Iss. 23, 2008-12 ,pp. : 3663-3674

Oxford University Press

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A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

By Malicdan May Christine V.   Noguchi Satoru   Nonaka Ikuya   Hayashi Yukiko K.   Nishino Ichizo  

Human Molecular Genetics, Vol. 16, Iss. 2, 2007-01 ,pp. : 115-128

Oxford University Press

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A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27

By Plancoulaine Sabine   Gessain Antoine   Tortevoye Patricia   Boland-Auge Anne   Vasilescu Alexandre   Matsuda Fumihiko   Abel Laurent  

Human Molecular Genetics, Vol. 15, Iss. 22, 2006-11 ,pp. : 3306-3312

Oxford University Press

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A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21

By Chaïb Hassan   Kaplan Josseline   Gerber Sylvie   Vincent Christophe   Ayadi Hammadi   Slim Rima   Munnich Arnold   Weissenbach Jean   Petit Christine  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 27-31

Oxford University Press

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The Gene for Schnyder's Crystalline Corneal Dystrophy Maps to Human Chromosome 1p34.1–p36

By Shearman Amanda M.   Hudson Thomas J.   Andresen J. Michael   Wu Xiaoyun   Sohn Robert L.   Haluska Frank   Housman David E.   Weiss Jayne S.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1667-1672

Oxford University Press

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