Mechanisms of Disease: a molecular genetic update on hereditary axonal neuropathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/ncpneuro0071.pdf
Reference59 articles.
1. Skre H (1974) Genetic and clinical aspects of CMT disease. Clin Genet 6: 78–118
2. Inherited Peripheral Neuropathies Mutation Database [ http://www.molgen.ua.ac.be/CMTMutations ]
3. Ben Othmane K et al. (1993) Localization of a gene (CMT2A) for autosomal dominant Charcot–Marie–Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics 17: 1–6
4. Züchner S et al. (2004) Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot–Marie–Tooth neuropathy type 2A. Nat Genet 36: 449–451
5. Lawson VH et al. (2005) Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene. Neurology 65: 197–204
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