Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting
Author:
Publisher
Wiley
Subject
Genetics,Animal Science and Zoology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2052.2006.01505.x/fullpdf
Reference6 articles.
1. Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1
2. Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization
3. Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.
4. 5 R. W. Miller (1965 ) Appaloosa Coat Color Inheritance . Dissertation, Bozeman, Montana State University, pp. 13 -25 .
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3. Investigation of HERC2 and OCA2 SNP for iris color variation in puerto rican paso fino horses;Journal of Equine Veterinary Science;2011-05
4. Pleiotropic effects of pigmentation genes in horses;Animal Genetics;2010-11-10
5. Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus);Genetics;2008-08-01
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