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Neurofilament light chain polypeptide gene mutations in Charcot–Marie–Tooth disease: nonsense mutation probably causes a recessive phenotype

Neurodegenerative DiseasesMolecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsRecessive PhenotypeMolecular BiologyCharcot–marie–tooth DiseaseDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationNonsense MutationMedicineNeurogenetics