OMIA:000819-9796 : Prekallikrein deficiency in Equus caballus (horse) |
In other species: dog
Categories: Haematopoietic system phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 229000 (gene) , 612423 (trait)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: In humans also called Fletcher factor deficiency
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000819-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 2021 | Dahlgren, A.R., Tablin, F., Finno, C.J. : |
| Genetics of equine bleeding disorders. Equine Vet J 53:30-37, 2021. Pubmed reference: 32463964. DOI: 10.1111/evj.13290. | |
| 1990 | Geor, R.J., Jackson, M.L., Lewis, K.D., Fretz, P.B. : |
| Prekallikrein deficiency in a family of Belgian horses. Journal of the American Veterinary Medical Association 197:741-745, 1990. Pubmed reference: 2211324. | |
| 1986 | Turrentine, M.A., Sculley, P.W., Green, E.M., Johnson, G.S. : |
| Prekallikrein deficiency in a family of miniature horses American Journal of Veterinary research 47:2464-2467, 1986. Pubmed reference: 3641551. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005