Brief communication. Shorn (shn): a new mutation causing hypotrichosis in the Norway rat

Publisher Website
Google Scholar
Abstract
We report the identification of an autosomal recessive mutation in the Norway rat that causes an almost complete absence of normal hair. The mutation, named shorn (gene symbol shn), is distinct from fuzzy, hairless, and Rowett nude, and is not closely linked with any of these markers or with albino.

This publication has 0 references indexed in Scilit: