TY  - GEN
AU  - Mizrahi-Meissonnier,Liliana
AU  - Merin,Saul
AU  - Banin,Eyal
AU  - Sharon,Dror
TI  - Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array
SN  - 1552-5783
PY  - 2010///0820
KW  - Adolescent
KW  - Adult
KW  - Amino Acid Sequence
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - Color Perception Tests
KW  - Color Vision Defects
KW  - genetics
KW  - Cone Opsins
KW  - DNA Mutational Analysis
KW  - Electroretinography
KW  - Female
KW  - Genes, X-Linked
KW  - Genetic Diseases, X-Linked
KW  - Heterozygote
KW  - Humans
KW  - Jews
KW  - Male
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Nystagmus, Pathologic
KW  - Pedigree
KW  - Phenotype
KW  - Retinal Degeneration
KW  - Tomography, Optical Coherence
KW  - Visual Acuity
KW  - physiology
KW  - Visual Fields
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1167/iovs.09-4592
ER  -