A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1. (2012)

First Author: Raja Rayan DL

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e318259e19c

PubMed Identifier: 22649220

Publication URI: http://europepmc.org/abstract/MED/22649220

Type: Journal Article/Review

Volume: 78

Parent Publication: Neurology

Issue: 24

ISSN: 0028-3878