A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.

Retinal photoreceptor dystrophies (RD) are a highly heterogeneous group of genetic disorders of the retina, representing the most frequently inherited form of visual handicap, affecting approximately 1.5 million people world wide. To date, more than 40 genetic loci have been implicated in RD. One of...

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Détails bibliographiques
Auteurs principaux: Papaioannou, M, Bessant, D, Payne, A, Bellingham, J, Rougas, C, Loutradis-Anagnostou, A, Gregory-Evans, C, Balassopoulou, A, Bhattacharya, S
Format: Artigo
Langue:Inglês
Publié: 1998
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051321/
https://ncbi.nlm.nih.gov/pubmed/9610810
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