TorsinA immunoreactivity in brains of patients with DYT1 and non-DYT1 dystonia
A mutation of the DYT1 gene, which codes for torsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. TorsinA immunohistochemistry was used to examine a case of DYT1, and several cases of non-DYT1, dystonia. No evidence was found for alterations of immunoreac...
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Veröffentlicht in: | Neurology 2002-01, Vol.58 (1), p.120-124 |
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