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Author reply: To PMID 24480711.
Halford, Stephanie; Liew, Gerald; Mackay, Donna S; Sergouniotis, Panagiotis I; Holt, Richard; Broadgate, Suzanne; Volpi, Emanuela V; Ocaka, Louise; Robson, Anthony G; Holder, Graham E; Moore, Anthony T; Michaelides, Michel; Webster, Andrew R.
Afiliação
  • Halford S; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK. Electronic address: stephanie.halford@ndcn.ox.ac.uk.
  • Liew G; Centre for Vision Research, Westmead Millennium Institute, University of Sydney, Sydney, Australia; Moorfields Eye Hospital, London, UK.
  • Mackay DS; Moorfields Eye Hospital, London, UK.
  • Sergouniotis PI; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
  • Holt R; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
  • Broadgate S; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
  • Volpi EV; Molecular Cytogenetics and Microscopy Core, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Ocaka L; Institute of Child Health, London, UK.
  • Robson AG; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
  • Holder GE; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
  • Moore AT; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
  • Michaelides M; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
  • Webster AR; Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.
Ophthalmology ; 122(4): e22, 2015 Apr.
Article em En | MEDLINE | ID: mdl-25797088
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Distrofias Hereditárias da Córnea / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Sistema Enzimático do Citocromo P-450 Limite: Female / Humans / Male Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Distrofias Hereditárias da Córnea / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Sistema Enzimático do Citocromo P-450 Limite: Female / Humans / Male Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article