Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats. [electronic resource]
Producer: 20060223Description: 222-4 p. digitalISSN:- 1087-0024
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural
There are no comments on this title.
Log in to your account to post a comment.