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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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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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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Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells

By Scheffers Martijn S.   vander Bent Paola   Prins Frans   Spruit Lia   Breuning MartijnH.   Litvinov SergeyV.   deHeer Emile   Peters DorienJ.M.  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2743-2750

Oxford University Press

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