HINT1 Mutations Cause Neuromyotonia in Greek Patients with CMT
source: pixabay.com

HINT1 Mutations Cause Neuromyotonia in Greek Patients with CMT

According to Charcot-Marie-Tooth News, researchers have associated HINT1 gene mutations with neuropathy in Greek patients with Charcot-Marie-Tooth disease (CMT). In the past, HINT1 was linked to CMT in central and southeastern Europe. However, researchers…

Continue Reading HINT1 Mutations Cause Neuromyotonia in Greek Patients with CMT