A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome. (2015)

First Author: Dusl M
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddv090

PubMed Identifier: 25765662

Publication URI: http://europepmc.org/abstract/MED/25765662

Type: Journal Article/Review

Volume: 24

Parent Publication: Human molecular genetics

Issue: 12

ISSN: 0964-6906