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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Mutations in a novel gene, VMD2 , encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)

By Passmore L.A.   Krämer F.   Rivera A.   Weber B.H.F.   Marquardt A.   Stöhr H.  

Human Molecular Genetics, Vol. 7, Iss. 9, 1998-09 ,pp. : 1517-1525

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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Disruption of the WFS1 gene in mice causes progressive -cell loss and impaired stimulus–secretion coupling in insulin secretion

By Ishihara Hisamitsu   Takeda Satoshi   Tamura Akira   Takahashi Rui   Yamaguchi Suguru   Takei Daisuke   Yamada Takahiro   Inoue Hiroshi   Soga Hiroyuki   Katagiri Hideki   Tanizawa Yukio   Oka Yoshitomo  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1159-1170

Oxford University Press

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Targeted disruption of Slc19a2 , the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice

By Forrest D.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2951-2960

Oxford University Press

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