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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

By Wayne Sigrid   Der Kaloustian Vazken M.   Schloss Melvin   Polomeno Robert   Scott Daryl A.   Hejtmancik J. Fielding   Sheffield Val C.   Smith Richard J. H.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1689-1692

Oxford University Press

Access to resources Recommend Favorite