A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

By Chavali Venkata R.M.   Khan Naheed W.   Cukras Catherine A.   Bartsch Dirk-Uwe   Jablonski Monica M.   Ayyagari Radha  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 2000-2014

Oxford University Press

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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 Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10 , Maps to Chromosome 6

By O'Neill Marsha E.   Marietta Jacquie   Nishimura Darryl   Wayne Sigrid   Van Camp Guy   Van Laer Lut   Negrini Clelia   Wilcox Edward R.   Chen Achih   Fukushima Kunihiro   Ni Li   Sheffield Val C.   Smith Richard J. H.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 853-856

Oxford University Press

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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Inner ear localization of mRNA and protein products of COCH , mutated in the sensorineural deafness and vestibular disorder, DFNA9

By Robertson N.G.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2493-2500

Oxford University Press

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