Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations. (2011)

First Author: Polke JM

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e3182242d4d

PubMed Identifier: 21715711

Publication URI: http://europepmc.org/abstract/MED/21715711

Type: Journal Article/Review

Volume: 77

Parent Publication: Neurology

Issue: 2

ISSN: 0028-3878