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Academic Journal

Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype.

  • Authors : Perrault I; Unité de Recherches Génétique et Epigénétique des Maladies Métaboliques, Neurosensorielles et du Développement (INSERM U781)- Université Paris Descartes- Fondation IMAGINE, Paris, France.; Estrada-Cuzcano A

Subjects: Mutation*; Eye Proteins/Eye Proteins/Eye Proteins/*genetics ; Leber Congenital Amaurosis/Leber Congenital Amaurosis/Leber Congenital Amaurosis/*genetics

  • Source: PloS one [PLoS One] 2013; Vol. 8 (1), pp. e51622. Date of Electronic Publication: 2013 Jan 07.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Periodical

AMD news from ISPOR.

  • Source: PharmacoEconomics & Outcomes News. 6/14/2008, Issue 555, p3-3. 1p.

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  • 1-10 ل  51 نتائج ل ""Retinal degeneration""