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ARVO Annual Meeting Abstract July 2019

Phenotype variations of retinal dystrophies caused by mutations in the PDE6β gene (MIM#613801)

Le Meur Guylene; Pierre Lebranchu; Mathilde Giraud; Fanny Billaud; Beatrice BOCQUET; Marie-Noelle Delyfer; Didier Lacombe; Stéphane Bézieau; Isabelle Anne Meunier; Michel Weber

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4496. doi:

ARVO Annual Meeting Abstract July 2018

Prevalence of mutations in PDE6B gene in autosomal recessive retinitis pigmentosa in the aim of gene therapy

Jean-Yves Deslandes; Mathilde Giraud; Bertrand Isidor; Patricia Talarmain; Ingrid Maury; Severine Marconi; Guylene Le Meur; Michel Weber; Isabelle Meunier; Christian Hamel; Stéphane Bezieau

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):38. doi:

ARVO Annual Meeting Abstract July 2018

A novel mutation in KIF3B in a family with dominant retinitis pigmentosa and polydactyly

Stephen P Daiger; Lori S Sullivan; Sara J Bowne; Elizabeth L Cadena; Kinga Maria Bujakowska; Eric A Pierce; Michael B Gorin; Xénia Latypova; Erica E Davis; Nicholas Katsanis; Ludovic Martin; Laurence Legeai-Mallet; Benjamin Cogne; Stéphane Bezieau; Thomas Besnard; Bertrand Isidor

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):47. doi:

ARVO Annual Meeting Abstract June 2013

Gene therapy in Leber congenital amaurosis due to rpe mutations: results of the first six patients included in a clinical trial

Guylene Le Meur; Pierre Lebranchu; Yann Péréon; Sebastien Schmitt; Stéphane Bézieau; Philippe Moullier; Fabienne Rolling; Michel Weber

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5969. doi:

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