| 1 | DICMT1, DNM2
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| Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation.
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| Gallardo E, Claeys KG, Nelis E, García A, Canga A, Combarros O, Timmerman V, De Jonghe P, Berciano J.
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| J Neurol 255(7):986-92. Epub 2008 Jun 17.
2008
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| 2 | DICMT1, DNM2
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| Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease.
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| Fabrizi GM, Ferrarini M, Cavallaro T, Cabrini I, Cerini R, Bertolasi L, Rizzuto N.
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| Neurology 69(3):291-5.
2007
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| 3 | DICMT1, DNM2, ZSWIM4
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| Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
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| Zuchner S, Noureddine M, Kennerson M, Verhoeven K, Claeys K, De Jonghe P, Merory J, Oliveira SA, Speer MC, Stenger JE, Walizada G, Zhu D, Pericak-Vance MA, Nicholson G, Timmerman V, Vance JM.
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| Nat Genet 37(3):289-94. Epub 2005 Jan 30. 2005
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| 4 | DICMT1
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| Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.
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| Speer MC, Graham FL, Bonner E, Collier K, Stajich JM, Gaskell PC, Pericak-Vance MA, Vance JM.
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| Neurogenetics 4(2):83-5. 2002
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| 5 | DICMT1
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| Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2.
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| Kennerson ML, Zhu D, Gardner RJ, Storey E, Merory J, Robertson SP, Nicholson GA.
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| Am J Hum Genet 69(4):883-8. 2001
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