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Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation (2019)

First Author: Thor M

Attributed to: Gene therapy for refractory epilepsy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41598-019-54041-0

PubMed Identifier: 31772215

Publication URI: http://europepmc.org/abstract/MED/31772215

Type: Journal Article/Review

Parent Publication: Scientific Reports

Issue: 1

ISSN: 2045-2322