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Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies.
Sheck, Leo; Davies, Wayne I L; Moradi, Phillip; Robson, Anthony G; Kumaran, Neruban; Liasis, Alki C; Webster, Andrew R; Moore, Anthony T; Michaelides, Michel.
Afiliación
  • Sheck L; Moorfields Eye Hospital, London, United Kingdom.
  • Davies WIL; UWA Oceans Institute, University of Western Australia, Crawley, Australia; School of Biological Sciences, University of Western Australia, Crawley, Australia; Lions Eye Institute, University of Western Australia, Crawley, Australia.
  • Moradi P; Moorfields Eye Hospital, London, United Kingdom; University College London Institute of Ophthalmology, University College London, United Kingdom.
  • Robson AG; Moorfields Eye Hospital, London, United Kingdom; University College London Institute of Ophthalmology, University College London, United Kingdom.
  • Kumaran N; Moorfields Eye Hospital, London, United Kingdom.
  • Liasis AC; Great Ormond Street Hospital, London, United Kingdom.
  • Webster AR; Moorfields Eye Hospital, London, United Kingdom; University College London Institute of Ophthalmology, University College London, United Kingdom.
  • Moore AT; Moorfields Eye Hospital, London, United Kingdom; University College London Institute of Ophthalmology, University College London, United Kingdom; Ophthalmology Department, School of Medicine, University of California San Francisco, San Francisco, California.
  • Michaelides M; Moorfields Eye Hospital, London, United Kingdom; University College London Institute of Ophthalmology, University College London, United Kingdom. Electronic address: michel.michaelides@moorfields.nhs.uk.
Ophthalmology ; 125(6): 894-903, 2018 06.
Article en En | MEDLINE | ID: mdl-29398085

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Amaurosis Congénita de Leber / Mutación / Antígenos de Neoplasias / Proteínas de Neoplasias Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ophthalmology Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Amaurosis Congénita de Leber / Mutación / Antígenos de Neoplasias / Proteínas de Neoplasias Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ophthalmology Año: 2018 Tipo del documento: Article