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

Hum Mutat. 2000 Jul;16(1):94. doi: 10.1002/1098-1004(200007)16:1<94::AID-HUMU25>3.0.CO;2-T.

Authors

E M Sankila¹, T H Joensuu, R H Hämäläinen, N Raitanen, O Valle, J Ignatius, B Cormand

Affiliation

¹ Department of Medical Genetics, University of Helsinki, Helsinki, Finland.

PMID: 10874321
DOI: 10.1002/1098-1004(200007)16:1<94::AID-HUMU25>3.0.CO;2-T

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Age of Onset
Child
Child, Preschool
Finland
Genes, Dominant / genetics*
Homeodomain Proteins / genetics*
Humans
Mutation / genetics*
Retinitis Pigmentosa / genetics*
Trans-Activators / genetics*

Substances

Homeodomain Proteins
Trans-Activators
cone rod homeobox protein