Your browser doesn't support javascript.
loading
Defects in the Cell Signaling Mediator ß-Catenin Cause the Retinal Vascular Condition FEVR.
Panagiotou, Evangelia S; Sanjurjo Soriano, Carla; Poulter, James A; Lord, Emma C; Dzulova, Denisa; Kondo, Hiroyuki; Hiyoshi, Atsushi; Chung, Brian Hon-Yin; Chu, Yoyo Wing-Yiu; Lai, Connie H Y; Tafoya, Mark E; Karjosukarso, Dyah; Collin, Rob W J; Topping, Joanne; Downey, Louise M; Ali, Manir; Inglehearn, Chris F; Toomes, Carmel.
Afiliación
  • Panagiotou ES; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Sanjurjo Soriano C; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Poulter JA; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Lord EC; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Dzulova D; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Kondo H; Department of Ophthalmology, Fukuoka University, Fukuoka 814-0180, Japan; Department of Ophthalmology, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.
  • Hiyoshi A; Department of Ophthalmology, Fukuoka University, Fukuoka 814-0180, Japan.
  • Chung BH; Department of Paediatrics and Adolescent Medicine, Centre for Genomic Sciences, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China.
  • Chu YW; Department of Paediatrics and Adolescent Medicine, Centre for Genomic Sciences, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China.
  • Lai CHY; Department of Ophthalmology, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China.
  • Tafoya ME; Pacific Retina Care, Waikele, HI 96797, USA.
  • Karjosukarso D; Department of Human Genetics and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, 6525 GA Nijmegen, the Netherlands.
  • Collin RWJ; Department of Human Genetics and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, 6525 GA Nijmegen, the Netherlands.
  • Topping J; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Downey LM; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK; Department of Ophthalmology, Hull Royal Infirmary, Hull HU3 2JZ, UK.
  • Ali M; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Inglehearn CF; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK.
  • Toomes C; Section of Ophthalmology & Neuroscience, Leeds Institute of Molecular Medicine, University of Leeds, Leeds LS9 7TF, UK. Electronic address: c.toomes@leeds.ac.uk.
Am J Hum Genet ; 100(6): 960-968, 2017 Jun 01.
Article en En | MEDLINE | ID: mdl-28575650
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Transducción de Señal / Beta Catenina Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Transducción de Señal / Beta Catenina Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article