MFN2 mutations cause severe phenotypes in most patients with CMT2A. (2011)

First Author: Feely SM

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e31821a441e

PubMed Identifier: 21508331

Publication URI: http://europepmc.org/abstract/MED/21508331

Type: Journal Article/Review

Volume: 76

Parent Publication: Neurology

Issue: 20

ISSN: 0028-3878