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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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

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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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A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21

By Chaïb Hassan   Kaplan Josseline   Gerber Sylvie   Vincent Christophe   Ayadi Hammadi   Slim Rima   Munnich Arnold   Weissenbach Jean   Petit Christine  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 27-31

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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