Wolfram syndrome 1 gene ( WFS1 ) product localizes to secretory granules and determines granule acidification in pancreatic -cells

By Hatanaka Masayuki   Tanabe Katsuya   Yanai Akie   Ohta Yasuharu   Kondo Manabu   Akiyama Masaru   Shinoda Koh   Oka Yoshitomo   Tanizawa Yukio  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1274-1284

Oxford University Press

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WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

By Takeda K.  

Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 477-484

Oxford University Press

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Mutations in the Wolfram syndrome 1 gene ( WFS1 ) are a common cause of low frequency sensorineural hearing loss

By Kurnool P.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2501-2508

Oxford University Press

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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An examination of wild-type SOD1 in modulating the toxicity and aggregation of ALS-associated mutant SOD1

By Prudencio Mercedes   Durazo Armando   Whitelegge Julian P.   Borchelt David R.  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4774-4789

Oxford University Press

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