OMIA 001889-452646 : Coat colour, talitsa in Neovison vison |
Mendelian trait/disorder:
yes
Mode of inheritance:
Autosomal Dominant
Considered a defect:
no
Key variant known:
no
Reference
1994 | Prasolova, L.A., Tichomirov, I.B., Vsevolodov, E.B., Latypov, I.F., Trapezov, O.V. : | |
Phenogenetic Analysis of Pigmentation of a New Coat Color Mutation of American Mink (Mustela vison schr L) and Its Combinations with Some of the Known Mutations Genetika 30:255-260, 1994. Pubmed reference: 8045387. |
Edit History
- Created by Frank Nicholas on 09 Nov 2013
- Changed by Frank Nicholas on 09 Nov 2013