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- [42] HINT1 neuropathy in Norway: clinical, genetic and functional profiling Orphanet Journal of Rare Diseases, 16
- [45] Lack of Neuropathy-Related Phenotypes in Hint1 Knockout Mice JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2014, 73 (07): : 693 - 701
- [48] Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy European Journal of Human Genetics, 2014, 22 : 847 - 850
- [49] The most common European HINT1 neuropathy variant phenotype and its case studies FRONTIERS IN NEUROLOGY, 2023, 14