Dyck P.J., Chance P., Lebo R., Carney J.A. (1993) Hereditary motor and sensory neuropathies., Dyck P.J., Thomas P.K., Griffin J.W., Low P.A., Podulso J.F. (Eds.), Peripheral neuropathy, Philadelphia: Saunders; 1094-1136.
Nelis E., Haites N., Van Broeckhoven C. (1999) Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. Hum. Mutat. 13:11-28.
Lupski J.R., Montes de Oca-Luna R., Slaugenhaupt S. (1991) DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 66:219-232.
Timmerman V., Nelis E., Van Hul W. (1992) The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nat. Genet. 1:171-175.
Hayasaka K., Himoro M., Sato W. (1993) Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat. Genet. 5:31-34.
Warner L.E., Hilz M.J., Appel S.H. (1996) Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth 1b, Dejerine-Sottas, and congenital hypomyelination. Neuron 17:451-460.
Lemke G. (1993) The molecular genetics of myelination: an update. Glia 7:263-271.
Wong M.H., Filbin M.T. (1996) Dominant-negative effect on adhesion by myelin Po protein truncated in its cytoplasmic domain. J. Cell Biol. 134:1531-1541.
Mandich P., Mancardi G.L., Varese A. (1999) Congenital hypomyelination due to myelin protein zero Q215X mutation. Ann. Neurol. 45:676-678.
Rautenstrauss B., Nelis E., Grehl H., Pfeiffer R.A., Van Broeckhoven C. (1994) Identification of a de novo insertional mutation in P0 in a patient with a Dejerine-Sottas syndrome (DSS) phenotype. Hum. Mol. Genet. 3:1701-1702.
Bellone E., Mandich P., James R., Nelis E., Lamba L.D., Van Broeckhoven C. (1996) Identification of a 4 bp deletion (1560del4) in P0 gene in a family with severe Charcot-Marie-Tooth disease. Hum. Mutat. 7:377-378.
Bort S., Nelis E., Timmerman V. (1997) Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. Hum. Genet. 99:746-754.
Nelis E., Timmerman V., De Jonghe P. (1994) Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene. Hum. Genet. 94:653-657.
Harding A.E., Thomas P.K. (1980) The clinical features of hereditary motor and sensory neuropathy type I and II. Brain 103:259-280.
Marques W., Hanna M.G., Marques S.R., Sweeney M.G., Thomas P.K., Wood N.W. (1999) Phenotypic variation of a new P0 mutation in genetically identical twins. J. Neurol. 246:596-599.