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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2017
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| Materias: | |
| 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 |