Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology,Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1385/NMM:8:1-2:43.pdf
Reference143 articles.
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3. Adlkofer K. Martini R., Aguzzi A. Zielasek J., Toyka K. V., and Suter U. (1995) Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nat. Genet. 11(3), 274–280.
4. Adlkofer K., Naef R., and Suter U. (1997b) Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele. J. Neurosci. Res., 49(6), 671–680.
5. Bellone E., Di Maria E., Soriani S. et al. (1999) A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease. Hum. Mutat. 14(4), 353–354.
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