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