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: | Llibre |
| Publicat: |
Pediatric Neurology Briefs Publishers,
1992-06-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Signatura: |
A1234.567 |
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| Còpia 1 | Disponible |