Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). [electronic resource]

By: Contributor(s): Producer: 20010111Description: 502-8 p. digitalISSN:
  • 1098-1004
Subject(s): Online resources: In: Human mutation vol. 16
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
No physical items for this record

Publication Type: Journal Article

There are no comments on this title.

to post a comment.