Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome. (2017)
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/10.1186/s13023-017-0732-z
PubMed Identifier: 29258548
Publication URI: http://europepmc.org/abstract/MED/29258548
Type: Journal Article/Review
Volume: 12
Parent Publication: Orphanet journal of rare diseases
Issue: 1
ISSN: 1750-1172