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

Human mutation

Volumn 16, Issue 1, 2000, Pages 94-

  Sankila, E M ^a   Joensuu, T H ^a   Hamalainen R H ^a   Raitanen, N ^a   Valle, O ^a   Ignatius, J ^a   Cormand, B ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

CONE ROD HOMEOBOX PROTEIN; HOMEODOMAIN PROTEIN; TRANSACTIVATOR PROTEIN;

ADOLESCENT; ARTICLE; CHILD; DOMINANT GENE; FINLAND; GENETICS; HUMAN; MUTATION; ONSET AGE; PRESCHOOL CHILD; RETINITIS PIGMENTOSA;

ADOLESCENT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; FINLAND; GENES, DOMINANT; HOMEODOMAIN PROTEINS; HUMANS; MUTATION; RETINITIS PIGMENTOSA; TRANS-ACTIVATORS;

EID: 0006549167     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200007)16:1<94::AID-HUMU25>3.0.CO;2-T     Document Type: Article

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