Autosomal recessive axonal neuropathy caused by HINT1 mutation: new association of a psychiatric disorder to the neurologic phenotype

In a recent paper Meng et al. [1] described three Chinese patients with autosomal recessive axonal neuropathy with neuromyotonia (ARAN-NM), caused by mutations in the histidine triad nucleotide binding protein (HINT1) gene.

Source: Neuromuscular Disorders - May 3, 2019 Category: Neurology Authors: Gaia Scarpini, Carlotta Spagnoli, Grazia Gabriella Salerno, Susanna Rizzi, Daniele Frattini, Carlo Fusco Tags: Letter to the Editor Source Type: research