Published 1992
| Version v1.0.0
Journal Article
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Hereditary Motor and Sensory Neuropathy Mutation
- Creators
- Millichap, J. Gordon
Abstract
A duplication in chromosome 17 responsible for most cases of autosomal dominant HMSN 1 was present as a de-novo mutation in 9 out of 10 sporadic patients examined at the Department of Neurology, Academic Medical Center, Amsterdam, The Netherlands.
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- PNB-6-44-a
- Created
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1992When the item was originally created.