A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

By Morton C.C.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 361-366

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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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with mutations – phenotypic spectrum and frequencies of mutations in Austria

By Janecke Andreas   Hirst-Stadlmann Almut   Günther Barbara   Utermann Barbara   Müller Thomas   Löffler Judith   Utermann Gerd   Nekahm-Heis Doris  

Human Genetics, Vol. 111, Iss. 2, 2002-08 ,pp. : 145-153

Springer Publishing Company

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Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre)

By Phelps P.D.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1105-1112

Oxford University Press

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Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss

By Meşe Gülistan   Londin Eric   Mui Rickie   Brink Peter   White Thomas  

Human Genetics, Vol. 115, Iss. 3, 2004-08 ,pp. : 191-199

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