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Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom

Hereditary NeuropathyRare DiseasesMendelian DisorderNeurological DisorderGenetic DisorderGeneticsUnderdiagnosed SymptomDegenerative DiseaseCzech PatientsNeuroscienceCommon DiseasesNeurologyDisease Gene IdentificationNeuropathologyMedicineNeurogenetics