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doi: 10.1016/j.psychres.2019.112727 154 KriSSzabCKelemenO

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An autosomal recessive form of hereditary axonal motor neuropathy associated with neuromyotonia has been linked to loss-of-function mutations of HINT1, which encodes histidine triad nucleotide-binding protein 1, a type of purine phosphoramidase