A dominant form of inherited retinal degeneration caused by a non-photoreceptor cell-specific mutation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 21, 1997, Pages 11645-11650

  Li, Lei ^a   Dowling, John E ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL SPECIFICITY; DOMINANT INHERITANCE; ELECTRORETINOGRAPHY; GENE MUTATION; LIGHT DARK CYCLE; NIGHT BLINDNESS; NONHUMAN; PHOTORECEPTOR CELL; PRIORITY JOURNAL; RETINA DEGENERATION; VISUAL NERVOUS SYSTEM; ZEBRA FISH;

ADAPTATION, OCULAR; AGING; ANIMALS; EMBRYO, NONMAMMALIAN; ESCAPE REACTION; FISH DISEASES; GENES, DOMINANT; HETEROZYGOTE DETECTION; MUTATION; NIGHT BLINDNESS; RETINA; RETINAL DEGENERATION; SENSORY THRESHOLDS; VISUAL ACUITY; ZEBRAFISH;

EID: 0030848814     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.21.11645     Document Type: Article

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