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Myasthenic syndromes due to defects in COL13A1 and in the N-linked glycosylation pathway. (2018)

First Author: Beeson D

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/10.1111/nyas.13576

PubMed Identifier: 29363764

Publication URI: http://europepmc.org/abstract/MED/29363764

Type: Journal Article/Review

Volume: 1413

Parent Publication: Annals of the New York Academy of Sciences

Issue: 1

ISSN: 0077-8923