Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2. (2008)

First Author: Houlden H

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/01.wnl.0000319696.14225.67

PubMed Identifier: 18832141

Publication URI: http://europepmc.org/abstract/MED/18832141

Type: Journal Article/Review

Volume: 71

Parent Publication: Neurology

Issue: 21

ISSN: 0028-3878