Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

By Fukuoka Hisakuni   Kanda Yukihiko   Ohta Shuji   Usami Shin-ichi  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 510-515

Springer Publishing Company

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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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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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Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product

By Hofmann S.  

Human Molecular Genetics, Vol. 12, Iss. 16, 2003-08 ,pp. : 2003-2012

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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