OMIA 001156-9913 : Spongiform myelopathy in Bos taurus |
Possibly relevant human trait(s) and/or gene(s) (MIM number):
271900
Mendelian trait/disorder:
unknown
Considered a defect:
yes
Inheritance:
As with spongiform encephelopathy, spongiform myelopathy is an aquired protein disorder.
Reference
| 1995 | Hindmarsh, M., Harper, P. : | |
| Congenital spongiform myelopathy of Simmental calves Australian Veterinary Journal 72:193-194, 1995. Pubmed reference: 7661822. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005