| 1 | CMTDID, CMT1B, CMT3A, MPZ |
| Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. | |
| Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. | |
| J Neurol Neurosurg Psychiatry 67(2):174-9. 1999 | |