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.
|1995||Hindmarsh, M., Harper, P. :|
|Congenital spongiform myelopathy of Simmental calves Australian Veterinary Journal 72:193-194, 1995. Pubmed reference: 7661822.|
- Created by Frank Nicholas on 06 Sep 2005