Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia. [electronic resource]

By: Contributor(s): Producer: 20031121Description: 525-8 p. digitalISSN:
  • 0387-7604
Subject(s): Online resources: In: Brain & development vol. 25
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

There are no comments on this title.

to post a comment.