Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting.
Abstract: No abstract available
Publication Date: 2006-09-19 PubMed ID: 16978190DOI: 10.1111/j.1365-2052.2006.01505.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Cite This Article
APA
Bellone R, Lawson S, Hunter N, Archer S, Bailey E.
(2006).
Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting.
Anim Genet, 37(5), 525.
https://doi.org/10.1111/j.1365-2052.2006.01505.x Publication
Researcher Affiliations
- Department of Biology, University of Tampa, Tampa, FL 33606, USA.
MeSH Terms
- Animals
- Exons
- Gene Frequency
- Genotype
- Hair Color / genetics
- Horses / genetics
- Polymorphism, Single Nucleotide
- Sequence Analysis, DNA
Citations
This article has been cited 2 times.- Bellone RR, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B. 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 Aug;179(4):1861-70.
- Sigurðardóttir H, Ablondi M, Kristjansson T, Lindgren G, Eriksson S. Genetic diversity and signatures of selection in Icelandic horses and Exmoor ponies. BMC Genomics 2024 Aug 8;25(1):772.
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