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

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Bibliographic Details
Published in:Human mutation 2000-07, Vol.16 (1), p.94-94
Main Authors: Sankila, Eeva-Marja, Joensuu, Tarja H., Hämäläinen, Riikka H., Raitanen, Nina, Valle, Olavi, Ignatius, Jaakko, Cormand, Bru
Format: Article
Language:English
Subjects:
Adolescent
Age of Onset
Child
Child, Preschool
cone-rod dystrophy
CRX
E80K
Finland
Genes, Dominant - genetics
Homeodomain Proteins - genetics
Humans
Mutation - genetics
Retinitis Pigmentosa - genetics
Trans-Activators - genetics
Online Access:Get full text
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ISSN:1059-7794
1098-1004
DOI:10.1002/1098-1004(200007)16:1<94::AID-HUMU25>3.0.CO;2-T