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  • Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 15, p. 2405, doi. 10.1093/hmg/ddn140
    By:
    • Jacobson, Samuel G.;
    • Cideciyan, Artur V.;
    • Aleman, Tomas S.;
    • Sumaroka, Alexander;
    • Roman, Alejandro J.;
    • Gardner, Leigh M.;
    • Prosser, Haydn M.;
    • Mishra, Monalisa;
    • Bech-Hansen, N. Torben;
    • Herrera, Waldo;
    • Schwartz, Sharon B.;
    • Liu, Xue-Zhong;
    • Kimberling, William J.;
    • Steel, Karen P.;
    • Williams, David S.
    Publication type:
    Article