TY  - GEN
AU  - Ponjavic,V
AU  - Abrahamson,M
AU  - Andréasson,S
AU  - Ehinger,B
AU  - Fex,G
AU  - Polland,W
TI  - A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu
SN  - 1381-6810
PY  - 1997///0916
KW  - Adult
KW  - Chromosome Aberrations
KW  - Chromosome Disorders
KW  - Electroretinography
KW  - Exons
KW  - genetics
KW  - Eye Diseases, Hereditary
KW  - Family Health
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Testing
KW  - Heterozygote
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Pedigree
KW  - Phenotype
KW  - Point Mutation
KW  - Proline
KW  - Retinitis Pigmentosa
KW  - Rhodopsin
KW  - Sequence Analysis, DNA
KW  - Sweden
KW  - Visual Acuity
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
ER  -