Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

By Mitchem K.L.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1887-1898

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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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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Hearing loss in a mouse model of Muenke syndrome

By Mansour Suzanne L.   Twigg Stephen R.F.   Freeland Rowena M.   Wall Steven A.   Li Chaoying   Wilkie Andrew O.M.  

Human Molecular Genetics, Vol. 18, Iss. 1, 2009-01 ,pp. : 43-50

Oxford University Press

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Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans

By Hwang Chan-Ho   Wu Doris K.  

Human Molecular Genetics, Vol. 17, Iss. 6, 2008-03 ,pp. : 844-853

Oxford University Press

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