Abstract
Equine osteochondrosis is a developmental joint disease that is a significant source of morbidity affecting multiple breeds of horse. The genetic variants underlying osteochondrosis susceptibility have not been established. Here, we describe the results of a genome-wide association study of osteochondrosis using 90 cases and 111 controls from a population of Dutch Warmblood horses. We report putative associations between osteochondrosis and loci on chromosome 3 (BIEC2-808543; P = 5.03 × 10(-7) ) and chromosome 10 (BIEC2-121323; P = 2.62 × 10(-7) ).
| Original language | English |
|---|---|
| Pages (from-to) | 408-12 |
| Number of pages | 5 |
| Journal | Animal Genetics |
| Volume | 44 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Aug 2013 |
| Externally published | Yes |
Keywords
- Animals
- Breeding
- Chromosome Mapping
- Chromosomes, Mammalian
- Female
- Genetic Loci
- Genetic Predisposition to Disease
- Genome-Wide Association Study
- Genotype
- Haplotypes
- Horse Diseases
- Horses
- Joint Diseases
- Male
- Osteochondrosis
- Phenotype
- Polymorphism, Single Nucleotide
- Radiography
- Journal Article
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