How to use the speech recognition tool?
Il Centro di riferimento per i disturbi rari nella genetica oftalmica (CARGO) è stato creato nel Piano Nazionale Malattie Rare nel novembre 2004. Accoglie bambini, adulti, coppie o famiglie interessate o suscettibili di essere affetti da una malattia oftalmica di origine genetica.
Gli obiettivi del centro sono:
Hélène Dollfus, Chair of TWG9, TWG10, member of WG1, WG2, WG3, WG5, WG6, WG7, WG8, WG9, WG10
Y. Perdomo, member of WG1, WG3, TWG8
D. Gaucher, member of WG1
J. De Seze, member of WG2
C. Speeg, member of WG3
F. Studer, member of TWG5
J. Muller, member of TWG6, TWG8
D. Leroux, member of TWG9, TWG10
Professor of Universities and Hospital Practitioner (PU-PH) in Medical Genetics and Ophthalmology. Head of the Medical Genetics Department of the Strasbourg University Hospitals (HUS), Coordinator of the Rare Diseases in Ophthalmic Genetics Reference Center (CARGO), as well as the national rare diseases branche SENSGENE, Director of the Medical Genetics Laboratory, Instigator of the future Institute of Medical Genetics of Alsace (IGMA), President of the scientific council of Retina France and Coordinator of the project ERN-EYE
CARGO, Hôpitaux Universitaires de Strasbourg
Tel : 0033 3 88 11 67 55