Publication | Closed Access
Dejerine–Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
254
Citations
34
References
1993
Year
Mendelian DisorderNeurological DisorderGenetic DisorderGeneticsPoint MutationDegenerative DiseaseDejerine–sottas SyndromeNeurologyPeripheral NervesMedicineNeuropathologyNeurogenetics
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