Performance of Swedish Warmblood fragile foal syndrome carriers and breeding prospects

BACKGROUND: Warmblood fragile foal syndrome (WFFS) is a monogenetic defect caused by a recessive lethal missense point mutation in the procollagen‐lysine, 2‐oxoglutarate 5‐dioxygenase 1 gene (PLOD1, c.2032G>A). The majority of homozygous WFFS horses are aborted during gestation. Clinical signs of...

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Detalles Bibliográficos
Autores principales: Ablondi, Michela, Johnsson, Martin, Eriksson, Susanne, Sabbioni, Alberto, Viklund, Åsa Gelinder, Mikko, Sofia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783495/
https://www.ncbi.nlm.nih.gov/pubmed/35062868
http://dx.doi.org/10.1186/s12711-021-00693-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783495/
https://www.ncbi.nlm.nih.gov/pubmed/35062868
http://dx.doi.org/10.1186/s12711-021-00693-4

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