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New agreement to facilitate genetic diagnosis of hereditary retinal dystrophies
An agreement between the University of Barcelona spin-off DBGen Ocular Genomics and the company Novartis EspaƱa will enable the genetic identification of retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA) in affected patients.
Comunidad autonoma de cataluna
Novartis espa
Megan craig
Rebeca valero
Roser gonz
Gemma marfany
European union
Department of genetics
University of barcelona
Institute of biomedicine
Ocular genomics
Leber congenital amaurosis
Retinitis pigmentosa
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