• HINT1 neuropathy in Norway: clinical, genetic and functional profiling 

      Høyer, Helle; Amor-Barris, Silvia; Brauteset, Lin; De Vriendt, Els; Strand, Linda; Jordanova, Albena; Braathen, Geir Julius; Peeters, Kristien (Peer reviewed; Journal article, 2021)
      Background: Autosomal recessive axonal neuropathy with neuromyotonia has been linked to loss of functional HINT1. The disease is particularly prevalent in Central and South-East Europe, Turkey and Russia due to the high ...