The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene. (2011)

First Author: Reilich P

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-011-6055-4

PubMed Identifier: 21544567

Publication URI: http://europepmc.org/abstract/MED/21544567

Type: Journal Article/Review

Volume: 258

Parent Publication: Journal of neurology

Issue: 11

ISSN: 0340-5354