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Clinical and Genetic Findings in CTNNA1-Associated Macular Pattern Dystrophy.
Tanner, Alexander; Chan, Hwei Wuen; Pulido, Jose S; Arno, Gavin; Ba-Abbad, Rola; Jurkute, Neringa; Robson, Anthony G; Egan, Catherine A; Knight, Hannah; Calcagni, Antonio; Taylor, Rachel L; Lenassi, Eva; Black, Graeme C; Moore, Anthony T; Michaelides, Michel; Webster, Andrew R; Mahroo, Omar A.
Afiliación
  • Tanner A; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Chan HW; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom; Department of Ophthalmology, National University Hospital, Singapore, Republic of Singapore.
  • Pulido JS; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom; Retina Service and Vickie and Jack Farber Vision Research Center, Wills Eye Hospital, Philadelphia, Pennsylvania.
  • Arno G; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Ba-Abbad R; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Jurkute N; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Robson AG; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Egan CA; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Knight H; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Calcagni A; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Taylor RL; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester, United Kingdom; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicines and Health, University of Manchester, Manchester, United Kingdom.
  • Lenassi E; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester, United Kingdom; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicines and Health, University of Manchester, Manchester, United Kingdom.
  • Black GC; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester, United Kingdom; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicines and Health, University of Manchester, Manchester, United Kingdom.
  • Moore AT; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom; Department of Ophthalmology, University of California, San Francisco, School of Medicine, San Francisco, California.
  • Michaelides M; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Webster AR; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom.
  • Mahroo OA; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Moorfields Eye Hospital, London, United Kingdom; Section of Ophthalmology, King's College London, St. Thomas' Hospital, London, United Kingdom; Physiology, Development and Neuroscience, University of Cambridge, Cambri
Ophthalmology ; 128(6): 952-955, 2021 06.
Article en En | MEDLINE | ID: mdl-33137351
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Alfa Catenina / Degeneración Macular / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Ophthalmology Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Alfa Catenina / Degeneración Macular / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Ophthalmology Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos