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Animal genetics2015; 46(5); 585-586; doi: 10.1111/age.12301

Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds.

Abstract: No abstract available
Publication Date: 2015-05-22 PubMed ID: 25997467DOI: 10.1111/age.12301Google Scholar: Lookup
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  • Journal Article

Cite This Article

APA
Petersen JL, Mickelson JR, Valberg SJ, McCue ME. (2015). Genome-wide SNP data show little differentiation between the Appaloosa and other American stock horse breeds. Anim Genet, 46(5), 585-586. https://doi.org/10.1111/age.12301

Publication

ISSN: 1365-2052
NlmUniqueID: 8605704
Country: England
Language: English
Volume: 46
Issue: 5
Pages: 585-586

Researcher Affiliations

Petersen, Jessica L
  • Department of Animal Science, University of Nebraska - Lincoln, Lincoln, NE, 68583-0908, USA.
Mickelson, James R
  • Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN, 55108, USA.
Valberg, Stephanie J
  • Veterinary Population Medicine, University of Minnesota, St. Paul, MN, 55108, USA.
McCue, Molly E
  • Veterinary Population Medicine, University of Minnesota, St. Paul, MN, 55108, USA.

MeSH Terms

  • Animals
  • Breeding
  • Female
  • Genome
  • Hair Color / genetics
  • Horses / classification
  • Horses / genetics
  • Male
  • Pedigree
  • Polymorphism, Single Nucleotide

Citations

This article has been cited 2 times.
  1. Valberg SJ, Schultz AE, Finno CJ, Bellone RR, Hughes SS. Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse-related breeds with the MYH1(E321G) mutation.. J Vet Intern Med 2022 May;36(3):1152-1159.
    doi: 10.1111/jvim.16417pubmed: 35426178google scholar: lookup
  2. Valberg SJ, Henry ML, Herrick KL, Velez-Irizarry D, Finno CJ, Petersen JL. Absence of myofibrillar myopathy in Quarter Horses with a histopathological diagnosis of type 2 polysaccharide storage myopathy and lack of association with commercial genetic tests.. Equine Vet J 2023 Mar;55(2):230-238.
    doi: 10.1111/evj.13574pubmed: 35288976google scholar: lookup