Published 2005
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Journal Article
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Genetics of Stiff Child Syndrome
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Abstract
A Chinese boy with a DYT1 gene mutation presented with muscle stiffness, painful muscle spasms, myoclonus, and dystonia, compatible with stiff child syndrome, and is reported from Queen Mary Hospital, the University of Hong Kong.Files
PNB-19-88-a.pdf
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- PNB-19-88-a
Dates
- Created
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2005When the item was originally created.