Identification of a novel locus for a USH3 like syndrome combined with congenital cataract

Author:

Dad S,Østergaard E,Thykjaer T,Albrectsen A,Ravn K,Rosenberg T,Møller LB

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. Update on Usher syndrome;Saihan;Curr Opin Neurol,2009

2. A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21;Chaib;Hum Mol Genet,1997

3. USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23;Ahmed;Clin Genet,2008

4. Identification of candidate regions for a novel Usher syndrome type II locus;Rebeh;Mol Vis,2008

5. A syndrome with retinitis pigmentosa, progressive hearing impairment, vestibular dysfunction, and congenital cataract;Rosenberg;Acta Ophthalmol Scand Suppl,1996

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