R381 Demetz Syndrome (AX, axonopathie)
The Demetz syndrome is a severe neurological condition causing muscle weakness, loss of coordination, and eventual death in affected calves of Tyrol Grey and Blanco Orejinegro breeds, due to a recessive mutation in the MFN2 gene.
- The description claims that the condition causes muscle weakness, loss of coordination, and eventual death.
Specifications
- Ras
- Blanco Orejinegro, Tyrol Grey
- Chromosoom
- 16
- Gen
- MFN2
How AI sees this product
The more complete this product's details, the more confidently AI assistants can understand and recommend it.
68%