| Literature DB >> 11971098 |
G Kuhlenbäumer1, P Young, C Oberwittler, G Hünermund, A Schirmacher, K Domschke, B Ringelstein, F Stögbauer.
Abstract
Giant axonal neuropathy (GAN) is an autosomal recessive neurologic disorder clinically characterized by a severe polyneuropathy, CNS abnormalities, and characteristic tightly curled hair. Recently, mutations in the gigaxonin gene have been identified as the underlying genetic defect. The authors report two novel mutations confirming that GAN is caused by mutations in the gigaxonin gene and raise the question whether some mutations may cause a mild subclinical neuropathy.Entities:
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Year: 2002 PMID: 11971098 DOI: 10.1212/wnl.58.8.1273
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910