Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.

Molecular vision

Volumn 4, Issue , 1998, Pages 23-

  Aguirre, G D ^a   Baldwin, V ^a   Pearce Kelling, S ^a   Narfstrom K ^a   Ray, K ^a   Acland, G M ^a  

^a Department of Obstetrics Gynecology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; EYE PROTEIN; PROTEIN; RPE65 PROTEIN, BOS TAURUS; RPE65 PROTEIN, HUMAN; RPE65 PROTEIN, RAT;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; DOG; ELECTRORETINOGRAPHY; FOUNDER EFFECT; GENETICS; MOLECULAR CLONING; MOLECULAR GENETICS; MUTATION; NIGHT BLINDNESS; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PEDIGREE; PIGMENT EPITHELIUM; RETINA; RETINA DEGENERATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SWEDEN; UNITED STATES;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CARRIER PROTEINS; CLONING, MOLECULAR; DOGS; ELECTRORETINOGRAPHY; EYE PROTEINS; FOUNDER EFFECT; MOLECULAR SEQUENCE DATA; MUTATION; NIGHT BLINDNESS; PEDIGREE; PIGMENT EPITHELIUM OF EYE; PROTEINS; RETINA; RETINAL DEGENERATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SWEDEN; UNITED STATES;

EID: 0032582425     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (0)