Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR. (2013)

First Author: Zoltowska K
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23569079

Publication URI:

Type: Journal Article/Review

Volume: 22

Parent Publication: Human molecular genetics

Issue: 14

ISSN: 0964-6906