A novel DFNA5 mutation does not cause hearing loss in an Iranian family

By Laer Lut   Meyer Nicole   Malekpour Mahdi   Riazalhosseini Yasser   Moghannibashi Mahdi   Kahrizi Kimia   Vandevelde Ann   Alasti Fatemeh   Najmabadi Hossein   Camp Guy   Smith Richard  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 549-552

Springer Publishing Company

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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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Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)

By Luijendijk Mirjam   Wijk Erwin   Bischoff Anne   Krieger Elmar   Huygen Patrick   Pennings Ronald   Brunner Han   Cremers Cor   Cremers Frans   Kremer Hannie  

Human Genetics, Vol. 115, Iss. 2, 2004-07 ,pp. : 149-156

Springer Publishing Company

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Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment ( DFNA7 ) in a Large Norwegian Family

By Fagerheim T.   Nilssen Ø.   Raeymaekers P.   Brox V.   Moum T.   Elverland H. H.   Teig E.   Omland H. H.   Fostad G. K.   Tranebjærg L.  

Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1187-1191

Oxford University Press

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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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