Search Results - Griffoin, Jean-Michel

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  1. 1
    Mutation spectrum and splicing variants in the OPA1 gene

    Mutation spectrum and splicing variants in the OPA1 gene by DELETTRE, Cécile, GRIFFOIN, Jean-Michel, KAPLAN, Josseline, DOLLFUS, Hélène, LORENZ, Birgit, FAIVRE, Laurence, LENAERS, Guy, BELENGUER, Pascale, HAMEL, Christian P

    Published in Human genetics
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  2. 2
    X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1

    X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1 by Duval, Pierre-André, Marlhens, Françoise, Griffoin, Jean-Michel, Millet, Pierre, Arnaud, Bernard, Hamel, Christian P.

    Published in Human mutation
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  3. 3
    Novel Mutations in MYO7A and USH2A in Usher Syndrome

    Novel Mutations in MYO7A and USH2A in Usher Syndrome by Maubaret, Cécilia, Griffoin, Jean-Michel, Arnaud, Bernard, Hamel, Christian P.

    Published in Ophthalmic genetics
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  4. 4
    Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralin

    Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralin by LAVIGNE-REBILLARD, Mireille, DELPRAT, Benjamin, SURGET, Marie-Odile, GRIFFOIN, Jean-Michel, WEIL, Dominique, ARBONES, Mariona, VINCENT, Robert, HAMEL, Christian P

    Published in Neurogenetics
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    Retinal dystrophies caused by mutations in RPE65 : assessment of visual functions

    Retinal dystrophies caused by mutations in RPE65 : assessment of visual functions by HAMEL, Christian P, GRIFFOIN, Jean-Michel, LASQUELLEC, Laetitia, BAZALGETTE, Christian, ARNAUD, Bernard

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  6. 6
    Retinal dystrophies caused by mutations inRPE65: assessment of visual functions

    Retinal dystrophies caused by mutations inRPE65: assessment of visual functions by Hamel, Christian P, Griffoin, Jean-Michel, Lasquellec, Laetitia, Bazalgette, Christian, Arnaud, Bernard

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