Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene. (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/10.1016/j.nmd.2020.02.012
PubMed Identifier: 32360402
Publication URI: http://europepmc.org/abstract/MED/32360402
Type: Journal Article/Review
Volume: 30
Parent Publication: Neuromuscular disorders : NMD
Issue: 4
ISSN: 0960-8966