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Genotype-phenotype association in patients with SCN4A mutation. (2019)

First Author: El-Battrawy I

Attributed to: Periodic paralysis: from molecules to mice funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/s0140-6736(19)31298-x

PubMed Identifier: 31180026

Publication URI: http://europepmc.org/abstract/MED/31180026

Type: Journal Article/Review

Volume: 393

Parent Publication: Lancet (London, England)

Issue: 10188

ISSN: 0140-6736