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The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. (2019)

First Author: Rodríguez Cruz PM

Attributed to: Disease mechanisms and therapy for inherited disorders of the neuromuscular synapse. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awz107

PubMed Identifier: 31081514

Publication URI: http://europepmc.org/abstract/MED/31081514

Type: Journal Article/Review

Volume: 142

Parent Publication: Brain : a journal of neurology

Issue: 6

ISSN: 0006-8950