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Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations (2021)

First Author: Sun J

Attributed to: Progressive Muscular Weakness in Periodic Paralysis and Normal Ageing funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2021.03.014

PubMed Identifier: 33965302

Publication URI: http://europepmc.org/abstract/MED/33965302

Type: Journal Article/Review

Parent Publication: Neuromuscular Disorders

Issue: 9

ISSN: 0960-8966