An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle (Q27346734)
Jump to navigation
Jump to search
scientific article (publication date: 2011)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle |
scientific article (publication date: 2011) |
Statements
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle (English)
0 references
2011
0 references
6
0 references
4
0 references
e18931
0 references
15 April 2011
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference