Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome. [electronic resource]

By: Contributor(s): Producer: 20090618Description: 1019-23 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 149A
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: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.