Hayasaka K، Himoro M، Sawaishi Y، وآخرون (نوفمبر 1993). "De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)". Nat. Genet. ج. 5 ع. 3: 266–8. DOI:10.1038/ng1193-266. PMID:7506095.
Roa BB، Dyck PJ، Marks HG، Chance PF، Lupski JR (نوفمبر 1993). "Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene". Nat. Genet. ج. 5 ع. 3: 269–73. DOI:10.1038/ng1193-269. PMID:8275092.
Hayasaka K، Himoro M، Sawaishi Y، وآخرون (نوفمبر 1993). "De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)". Nat. Genet. ج. 5 ع. 3: 266–8. DOI:10.1038/ng1193-266. PMID:7506095.
Roa BB، Dyck PJ، Marks HG، Chance PF، Lupski JR (نوفمبر 1993). "Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene". Nat. Genet. ج. 5 ع. 3: 269–73. DOI:10.1038/ng1193-269. PMID:8275092.