A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H. (2009)

First Author: Houlden H

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/01.wnl.0000342463.35089.cc

PubMed Identifier: 19221294

Publication URI: http://europepmc.org/abstract/MED/19221294

Type: Journal Article/Review

Volume: 72

Parent Publication: Neurology

Issue: 7

ISSN: 0028-3878