Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel Gating
Human Mutation | July 4, 2016 | Volume: 37 | Issue: 10 | Pages: 1051-1059
10.1002/humu.23043
| PMID 27375219