Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3

Mammalian Genome

Volumn 20, Issue 2, 2009, Pages 109-123

  Kukekova, Anna V ^a   Goldstein, Orly ^a   Johnson, Jennifer L ^a   Richardson, Malcolm A ^a,b   Pearce Kelling, Susan E ^a   Swaroop, Anand ^c,d   Friedman, James S ^d   Aguirre, Gustavo D ^e   Acland, Gregory M ^a  

^a Department of Obstetrics Gynecology   (United States)

^b DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

^c UNIVERSITY OF MICHIGAN   (United States)

^d NATIONAL EYE INSTITUTE   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BREEDING; CODON; DOG; GENE; GENE INSERTION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENE MUTATION; GENETIC TRAIT; HAPLOTYPE; HOMOZYGOTE; MEIOSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; ORTHOLOGY; POPULATION STRUCTURE; PREDICTION; RD3 GENE; RNA SPLICING; ROD CONE DYSPLASIA TYPE 2;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DOG DISEASES; DOGS; EYE PROTEINS; HUMANS; LINKAGE DISEQUILIBRIUM; MICE; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEAR PROTEINS; PEDIGREE; RETINAL DYSPLASIA;

CANIS FAMILIARIS; MURINAE;

EID: 59649126704     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-008-9163-4     Document Type: Article

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