Your browser doesn't support javascript.
loading
North Carolina Macular Dystrophy: Phenotypic Variability and Computational Analysis of Disease-Associated Noncoding Variants.
Green, David J; Lenassi, Eva; Manning, Cerys S; McGaughey, David; Sharma, Vinod; Black, Graeme C; Ellingford, Jamie M; Sergouniotis, Panagiotis I.
Afiliación
  • Green DJ; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Lenassi E; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Manning CS; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • McGaughey D; Manchester Royal Eye Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Sharma V; Division of Developmental Biology and Medicine, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Black GC; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States.
  • Ellingford JM; Manchester Royal Eye Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Sergouniotis PI; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Invest Ophthalmol Vis Sci ; 62(7): 16, 2021 06 01.
Article en En | MEDLINE | ID: mdl-34125159
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Retina / Factores de Transcripción / Distrofias Hereditarias de la Córnea / N-Metiltransferasa de Histona-Lisina Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Retina / Factores de Transcripción / Distrofias Hereditarias de la Córnea / N-Metiltransferasa de Histona-Lisina Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2021 Tipo del documento: Article