Published 1992
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Hereditary Motor and Sensory Neuropathy Mutation
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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.Files
PNB-6-44-a.pdf
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- PNB-6-44-a
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- Created
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1992When the item was originally created.