A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle

BACKGROUND: Surveillance for bovine genetic diseases in Denmark identified a hitherto unreported congenital syndrome occurring among progeny of a Holstein sire used for artificial breeding. A genetic aetiology due to a dominant inheritance with incomplete penetrance or a mosaic germline mutation was...

Descripción completa

Detalles Bibliográficos
Autores principales: Agerholm, Jørgen S., McEvoy, Fintan J., Heegaard, Steffen, Charlier, Carole, Jagannathan, Vidhya, Drögemüller, Cord
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541750/
https://www.ncbi.nlm.nih.gov/pubmed/28768473
http://dx.doi.org/10.1186/s12863-017-0541-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541750/
https://www.ncbi.nlm.nih.gov/pubmed/28768473
http://dx.doi.org/10.1186/s12863-017-0541-3

Ejemplares similares