Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.

Mizrahi-Meissonnier, Liliana

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array. [electronic resource] - Investigative ophthalmology & visual science Aug 2010 - 3884-92 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1552-5783

10.1167/iovs.09-4592 doi


Adolescent
Adult
Amino Acid Sequence
Child
Child, Preschool
Chromosome Mapping
Color Perception Tests
Color Vision Defects--genetics
Cone Opsins--genetics
DNA Mutational Analysis
Electroretinography
Female
Genes, X-Linked
Genetic Diseases, X-Linked--genetics
Heterozygote
Humans
Jews--genetics
Male
Middle Aged
Molecular Sequence Data
Mutation
Nystagmus, Pathologic--genetics
Pedigree
Phenotype
Retinal Degeneration--genetics
Tomography, Optical Coherence
Visual Acuity--physiology
Visual Fields
Young Adult