Charcot-Marie-Tooth Disease: Seventeen Causative Genes

Abstract

Charcot-Marie-Tooth disease (CMT) is the most common form of inherited motor and sensory neuropathy. Moreover, CMT is a genetically heterogeneous disorder of the peripheral nervous system, with many genes identified as CMT-causative. CMT has two usual classifications: type 1, the demyelinating form (CMT1); and type 2, the axonal form (CMT2). In addition… (More)
DOI: 10.3988/jcn.2006.2.2.92

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