Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients. (2011)

First Author: Durmus H

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e318207b043

PubMed Identifier: 21242490

Publication URI: http://europepmc.org/abstract/MED/21242490

Type: Journal Article/Review

Volume: 76

Parent Publication: Neurology

Issue: 3

ISSN: 0028-3878