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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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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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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Interactions in the network of Usher syndrome type 1 proteins

By Adato Avital  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 347-356

Oxford University Press

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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

By Adato Avital   Lefèvre Gaëlle   Delprat Benjamin   Michel Vincent   Michalski Nicolas   Chardenoux Sébastien   Weil Dominique   El-Amraoui Aziz   Petit Christine  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3921-3932

Oxford University Press

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