Analysis of six candidate genes as potential modifiers of disease expression in canine XLPRA1, a model for human X-linked retinitis pigmentosa 3

por Guyon, Richard, Pearce-Kelling, Susan E., Zeiss, Caroline J., Acland, Gregory M., Aguirre, Gustavo D.
Publicado 2007

Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia

por Yeh, Connie Y, Goldstein, Orly, Kukekova, Anna V, Holley, Debbie, Knollinger, Amy M, Huson, Heather J, Pearce-Kelling, Susan E, Acland, Gregory M, Komáromy, András M
Publicado 2013

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

por 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.
Publicado 2010