The study enrolled CMT1A patients, whose disease was caused by a mutation in the PMP22 gene on chromosome 17. The Paris-based company said that the trial was scuppered by a high placebo response ...

Molecular mechanisms of TRPV4-mediated motor axon degeneration | Jeremy Sullivan, Ph.D. Efficient 4-factor induced Schwann (4FiS) cell platform for CMT1A modeling with macrophage-integrated neural ...

Correspondence to Georgios Koutsis, Neurogenetics Unit, 1st Department of Neurology, School of Medicine, Eginition Hospital, National and Kapodistrian University of Athens, Athens 11528, Greece; ...