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Shedding light on myopia by studying complete congenital stationary night blindness.
Zeitz, Christina; Roger, Jérome E; Audo, Isabelle; Michiels, Christelle; Sánchez-Farías, Nuria; Varin, Juliette; Frederiksen, Helen; Wilmet, Baptiste; Callebert, Jacques; Gimenez, Marie-Laure; Bouzidi, Nassima; Blond, Frederic; Guilllonneau, Xavier; Fouquet, Stéphane; Léveillard, Thierry; Smirnov, Vasily; Vincent, Ajoy; Héon, Elise; Sahel, José-Alain; Kloeckener-Gruissem, Barbara; Sennlaub, Florian; Morgans, Catherine W; Duvoisin, Robert M; Tkatchenko, Andrei V; Picaud, Serge.
Afiliação
  • Zeitz C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France. Electronic address: christina.zeitz@inserm.fr.
  • Roger JE; Paris-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, Saclay, France.
  • Audo I; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France; CHNO des Quinze-Vingts, INSERM-DGOS CIC 1423, Paris, France.
  • Michiels C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Sánchez-Farías N; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Varin J; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Frederiksen H; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Wilmet B; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Callebert J; Service of Biochemistry and Molecular Biology, INSERM U942, Hospital Lariboisière, APHP, Paris, France.
  • Gimenez ML; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Bouzidi N; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Blond F; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Guilllonneau X; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Fouquet S; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Léveillard T; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Smirnov V; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Vincent A; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada; Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, ON, Canada; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Héon E; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada; Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, ON, Canada; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Sahel JA; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France; CHNO des Quinze-Vingts, INSERM-DGOS CIC 1423, Paris, France; Department of Ophthalmology, The University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Kloeckener-Gruissem B; Department of Biology, ETH Zurich, Zurich, Switzerland.
  • Sennlaub F; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Morgans CW; Department of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR, USA.
  • Duvoisin RM; Department of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR, USA.
  • Tkatchenko AV; Oujiang Laboratory, Zhejiang Laboratory for Regenerative Medicine, Vision and Brain Health, Wenzhou, China; Department of Ophthalmology, Edward S. Harkness Eye Institute, Columbia University, New York, NY, USA.
  • Picaud S; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
Prog Retin Eye Res ; 93: 101155, 2023 03.
Article em En | MEDLINE | ID: mdl-36669906
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Cegueira Noturna / Doenças Genéticas Ligadas ao Cromossomo X / Miopia Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Cegueira Noturna / Doenças Genéticas Ligadas ao Cromossomo X / Miopia Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article