Warmblood fragile foal syndrome causative single nucleotide polymorphism frequency in horses in Ireland

BACKGROUND: Warmblood Fragile Foal Syndrome (WFFS) is an autosomal recessive disorder caused by a mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (PLOD1) gene. Homozygosity for the mutation results in defective collagen synthesis which clinically manifests as the birth of non viab...

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Detalles Bibliográficos
Autores principales: Rowe, Áine, Flanagan, Sharon, Barry, Gerald, Katz, Lisa M., Lane, Elizabeth A., Duggan, Vivienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524838/
https://www.ncbi.nlm.nih.gov/pubmed/34663462
http://dx.doi.org/10.1186/s13620-021-00206-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524838/
https://www.ncbi.nlm.nih.gov/pubmed/34663462
http://dx.doi.org/10.1186/s13620-021-00206-1

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