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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Detaylı Bibliyografya
Asıl Yazarlar: Papaioannou, M, Bessant, D, Payne, A, Bellingham, J, Rougas, C, Loutradis-Anagnostou, A, Gregory-Evans, C, Balassopoulou, A, Bhattacharya, S
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1998
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051321/
https://ncbi.nlm.nih.gov/pubmed/9610810
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