CHMP2B mutations are rare in French families with frontotemporal lobar degeneration. [electronic resource]

By: Contributor(s): Producer: 20111110Description: 2032-6 p. digitalISSN:
  • 1432-1459
Subject(s): Online resources: In: Journal of neurology vol. 257
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.