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By Mitchem K.L.  

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

Oxford University Press

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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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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

By Robertson Nahid G.   Jones Sherri M.   Sivakumaran Theru A.   Giersch Anne B.S.   Jurado Sara A.   Call Linda M.   Miller Constance E.   Maison Stphane F.   Liberman M. Charles   Morton Cynthia C.  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3426-3434

Oxford University Press

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Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)

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Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1709-1715

Oxford University Press

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Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

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Human Molecular Genetics, Vol. 15, Iss. 14, 2006-07 ,pp. : 2185-2191

Oxford University Press

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