Warmblood fragile foal syndrome type 1 mutation (PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed

BACKGROUND: Catastrophic fractures are among the most common cause of fatalities in racehorses. Several factors, including genetics, likely contribute to increased risk for fatal injuries. A variant in the procollagen‐lysine, 2‐oxoglutarate 5‐dioxygenase1 gene (PLOD1 c.2032G>A) was shown to cause...

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Detalles Bibliográficos
Autores principales: Bellone, R. R., Ocampo, N. R., Hughes, S. S., Le, V., Arthur, R., Finno, C. J., Penedo, M. C. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Surveys and Population Studies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062577/
https://www.ncbi.nlm.nih.gov/pubmed/31502696
http://dx.doi.org/10.1111/evj.13182

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062577/
https://www.ncbi.nlm.nih.gov/pubmed/31502696
http://dx.doi.org/10.1111/evj.13182

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