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

Rod cone dysplasia type 2 (rcd2) is an autosomal recessive disorder that segregates in collie dogs. Linkage disequilibrium and meiotic linkage mapping were combined to take advantage of population structure within this breed, and to fine map rcd2 to a 230 kb candidate region that included the gene C...

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Détails bibliographiques
Auteurs principaux: Kukekova, Anna V., Goldstein, Orly, Johnson, Jennifer L., Richardson, Malcolm A., Pearce-Kelling, Susan E., Swaroop, Anand, Friedman, James S., Aguirre, Gustavo D., Acland, Gregory M.
Format: Artigo
Langue:Inglês
Publié: 2009
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652121/
https://ncbi.nlm.nih.gov/pubmed/19130129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-008-9163-4
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