Aleutian mink

Show Summary Details

Quick Reference

An autosomal recessive mutation in Mustela vison producing diluted pigmentation of the fur and eyes. The homozygotes show a lysosomal defect similar in humans to the Chédiak-Higashi syndrome (q.v.).

Subjects: Genetics and Genomics.

Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.