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Multiethnic involvement in autosomal-dominant optic atrophy in Singapore.
Loo, J L; Singhal, S; Rukmini, A V; Tow, S; Amati-Bonneau, P; Procaccio, V; Bonneau, D; Gooley, J J; Reynier, P; Ferré, M; Milea, D.
Afiliación
  • Loo JL; Department of Neuro-Ophthalmology, Singapore National Eye Centre, Singapore, Singapore.
  • Singhal S; Department of Neuro-Ophthalmology, Singapore National Eye Centre, Singapore, Singapore.
  • Rukmini AV; Singapore Eye Research Institute, Singapore, Singapore.
  • Tow S; Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Amati-Bonneau P; Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Procaccio V; Department of Neuro-Ophthalmology, Singapore National Eye Centre, Singapore, Singapore.
  • Bonneau D; Department of Biochemistry and Genetics, UMR CNRS6214-INSERM1083, University Hospital of Angers, Angers, France.
  • Gooley JJ; Department of Biochemistry and Genetics, UMR CNRS6214-INSERM1083, University Hospital of Angers, Angers, France.
  • Reynier P; Department of Biochemistry and Genetics, UMR CNRS6214-INSERM1083, University Hospital of Angers, Angers, France.
  • Ferré M; Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Milea D; Department of Biochemistry and Genetics, UMR CNRS6214-INSERM1083, University Hospital of Angers, Angers, France.
Eye (Lond) ; 31(3): 475-480, 2017 Mar.
Article en En | MEDLINE | ID: mdl-27858935

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Atrofia Óptica Autosómica Dominante / GTP Fosfohidrolasas / Mutación Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Eye (Lond) Asunto de la revista: OFTALMOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Singapur Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Atrofia Óptica Autosómica Dominante / GTP Fosfohidrolasas / Mutación Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Eye (Lond) Asunto de la revista: OFTALMOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Singapur Pais de publicación: Reino Unido