Congenital myasthenic syndrome due to mutations in MUSK suggests that the level of MuSK phosphorylation is crucial for governing synaptic structure. (2020)
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/10.1002/humu.23949
PubMed Identifier: 31765060
Publication URI: http://europepmc.org/abstract/MED/31765060
Type: Journal Article/Review
Volume: 41
Parent Publication: Human mutation
Issue: 3
ISSN: 1059-7794