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Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.
Paunescu, K; Preising, M N; Janke, B; Wissinger, B; Lorenz, B.
  • Paunescu K; Department of Pediatric Ophthalmology, Strabismology, and Ophthalmogenetics, Klinikum, University of Regensburg, Regensburg, Germany.
Ophthalmology ; 114(7): 1348-1357.e1, 2007 Jul.
Article en En | MEDLINE | ID: mdl-17320181
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Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Transactivadores / Sistemas de Lectura Abierta / Proteínas de Homeodominio / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Aged / Female / Humans / Male Idioma: En Año: 2007 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Transactivadores / Sistemas de Lectura Abierta / Proteínas de Homeodominio / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Aged / Female / Humans / Male Idioma: En Año: 2007 Tipo del documento: Article