Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)

The appaloosa coat spotting pattern in horses is caused by a single incomplete dominant gene (LP). Homozygosity for LP (LP/LP) is directly associated with congenital stationary night blindness (CSNB) in Appaloosa horses. LP maps to a 6-cM region on ECA1. We investigated the relative expression of tw...

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Detalhes bibliográficos
Main Authors: Bellone, Rebecca R., Brooks, Samantha A., Sandmeyer, Lynne, Murphy, Barbara A., Forsyth, George, Archer, Sheila, Bailey, Ernest, Grahn, Bruce
Formato: Artigo
Idioma:Inglês
Publicado em: Genetics Society of America 2008
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Investigations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2516064/
https://ncbi.nlm.nih.gov/pubmed/18660533
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.108.088807
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