Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter. (2021)
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/10.1016/j.nmd.2020.10.006
PubMed Identifier: 33250374
Publication URI: http://europepmc.org/abstract/MED/33250374
Type: Journal Article/Review
Volume: 31
Parent Publication: Neuromuscular disorders : NMD
Issue: 1
ISSN: 0960-8966