An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9

PURPOSE: To identify the causative mutation in a canine cone-rod dystrophy (crd3) that segregates as an adult onset disorder in the Glen of Imaal Terrier breed of dog. METHODS: Glen of Imaal Terriers were ascertained for crd3 phenotype by clinical ophthalmoscopic examination, and in selected cases b...

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Autors principals: Goldstein, Orly, Mezey, Jason G., Boyko, Adam R., Gao, Chuan, Wang, Wei, Bustamante, Carlos D., Anguish, Lynne J., Jordan, Julie Ann, Pearce-Kelling, Susan E., Aguirre, Gustavo D., Acland, Gregory M.
Format: Artigo
Idioma:Inglês
Publicat: Molecular Vision 2010
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2925905/
https://ncbi.nlm.nih.gov/pubmed/20806078
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