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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PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

By Ahmed Zubair M.  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3215-3223

Oxford University Press

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Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

By Weil Dominique  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 463-471

Oxford University Press

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Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2

By Reiners Jan   van Wijk Erwin   Zimmermann Ulrike   Jürgens Karin   te Brinke Heleen   Overlack Nora   Roepman Ronald   Knipper Marlies   Kremer Hannie   Wolfrum Uwe  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3933-3943

Oxford University Press

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Myo15 function is distinct from Myo6 , Myo7a and pirouette genes in development of cochlear stereocilia

By Karolyi I. Jill  

Human Molecular Genetics, Vol. 12, Iss. 21, 2003-11 ,pp. : 2797-2805

Oxford University Press

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