Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia. [electronic resource]

By: Contributor(s): Producer: 20150512Description: 393-5 p. digitalISSN:
  • 1399-0004
Subject(s): Online resources: In: Clinical genetics vol. 85
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; Letter; Research Support, N.I.H., Intramural

There are no comments on this title.

to post a comment.