Hereditary Motor and Sensory Neuropathy Mutation
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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1992-06-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/3011 |