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Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.
Boulouiz, Redouane; Li, Yun; Abidi, Omar; Bolz, Hanno; Chafik, Abdelaziz; Kubisch, Christian; Roub, Hassan; Wollnik, Bernd; Barakat, Abdelhamid.
Affiliation
  • Boulouiz R; Department of Genetics, Institute Pasteur du Maroc, Casablanca, Morocco.
Mol Vis ; 13: 1862-5, 2007 Oct 02.
Article in En | MEDLINE | ID: mdl-17960123
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Database: MEDLINE Main subject: Myosins / Dyneins / Usher Syndromes / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2007 Type: Article Affiliation country: Morocco
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Database: MEDLINE Main subject: Myosins / Dyneins / Usher Syndromes / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2007 Type: Article Affiliation country: Morocco