- Title
- Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
- Creators - without role
- Maria Solaki - STZ eyetrialBritta Baumann - STZ eyetrialPeggy Reuter - STZ eyetrialSten Andreasson - Lund UniversityIsabelle Audo - InsermCarmen Ayuso - Centre for Biomedical Network Research on Rare DiseasesGhassan Balousha - Al-Quds UniversityFrancesco Benedicenti - Ospedale di BolzanoDavid Birch - Retina Foundation of the SouthwestPierre Bitoun - Hôpital Jean-VerdierDelphine Blain - National Eye InstituteBeatrice Bocquet - Université de Montpellier, Institut des Neurosciences de Montpellier - INMKari Branham - University of Michigan–Ann ArborJaume Català-Mora - Hospital Sant Joan de Déu BarcelonaElfride de Baere - Ghent University HospitalHelene Dollfus - Hôpitaux Universitaires de StrasbourgMohammed Falana - Al-Quds UniversityRoberto Giorda - IRCCS Eugenio MedeaIrina Golovleva - Umeå UniversityIrene Gottlob - UlverscroftJohn Heckenlively - University of Michigan–Ann ArborSamuel Jacobson - Penn Presbyterian Medical CenterKaylie JonesHerbert Jägle - University of RegensburgAndreas Janecke - Innsbruck Medical UniversityUlrich Kellner - ChondrometricsPetra Liskova - General University Hospital in PragueBirgit Lorenz - University of GiessenLoreto Martorell-SampolAndré Messias - Universidade de São PauloIsabelle Meunier - Université de Montpellier, Institut des Neurosciences de Montpellier - INMFernanda Belga Ottoni PortoEleni Papageorgiou - University Hospital of LarissaAstrid Plomp - University of AmsterdamThomy de RavelCharlotte ReiffAgnes Renner - Regensburg University of Applied SciencesThomas Rosenberg - Glostrup HospitalGünther Rudolph - Ludwig-Maximilians-Universität MünchenRoberto Salati - IRCCS Eugenio MedeaE. Cumhur SenerPaul Sieving - California Institute for Regenerative MedicineFranco Stanzial - Ospedale di BolzanoElias Traboulsi - Cleveland Eye ClinicStephen Tsang - Columbia UniversityBalázs Varsanyi - University of PecsRichard Weleber - Oregon Health & Science UniversityDitta Zobor - STZ eyetrialKatarina Stingl - University of TübingenBernd Wissinger - STZ eyetrialSusanne Kohl - STZ eyetrial
- Publication Details
- Human Mutation, Vol.43(7), pp.832-858
- Identifiers
- 9939691609311
- Academic Unit
- Institut des Neurosciences de Montpellier - INM
- Language
- English
- Resource Type
- Journal article
- Local Fields
- hal-04958878
Journal article
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
Human Mutation, Vol.43(7), pp.832-858
14/04/2022
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