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A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophy

✍ Scribed by Eeva-Marja Sankila; Tarja H. Joensuu; Riikka H. Hämäläinen; Nina Raitanen; Olavi Valle; Jaakko Ignatius; Bru Cormand

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 11 KB
Volume: 16
Category: Article
ISSN: 1059-7794
DOI: 10.1002/1098-1004(200007)16:1<94::aid-humu25>3.0.co;2-t

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