A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A. (2009)

First Author: Rajakulendran S

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e3181b87959

PubMed Identifier: 19770477

Publication URI: http://europepmc.org/abstract/MED/19770477

Type: Journal Article/Review

Volume: 73

Parent Publication: Neurology

Issue: 12

ISSN: 0028-3878