Usher syndromes due to MYO7A , PCDH15 , USH2A or GPR98 mutations share retinal disease mechanism

By Jacobson Samuel G.   Cideciyan Artur V.   Aleman Tomas S.   Sumaroka Alexander   Roman Alejandro J.   Gardner Leigh M.   Prosser Haydn M.   Mishra Monalisa   Bech-Hansen N. Torben   Herrera Waldo   Schwartz Sharon B.   Liu Xue-Zhong   Kimberling William J.   Steel Karen P.   Williams David S.  

Human Molecular Genetics, Vol. 17, Iss. 15, 2008-08 ,pp. : 2405-2415

Oxford University Press

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Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

By Bernier F.P.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1709-1718

Oxford University Press

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Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

By Johnson Kenneth R.   Gagnon Leona H.   Webb Lisa S.   Peters Luanne L.   Hawes Norman L.   Chang Bo   Zheng Qing Yin  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3075-3086

Oxford University Press

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

By Zelante Leopoldo   Gasparini Paolo   Estivill Xavier  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1605-1609

Oxford University Press

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The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

By van Wijk Erwin   van der Zwaag Bert   Peters Theo   Zimmermann Ulrike   te Brinke Heleen   Kersten Ferry F.J.   Märker Tina   Aller Elena   Hoefsloot Lies H.   Cremers Cor W.R.J.   Cremers Frans P.M.   Wolfrum Uwe   Knipper Marlies   Roepman Ronald  

Human Molecular Genetics, Vol. 15, Iss. 5, 2006-03 ,pp. : 751-765

Oxford University Press

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