Tyrosine hydroxylase and levodopa responsive dystonia
- PMID: 2565377
- PMCID: PMC1032668
- DOI: 10.1136/jnnp.52.1.112
Tyrosine hydroxylase and levodopa responsive dystonia
Abstract
It has been suggested that a form of inherited dystonia responsive to levodopa might be due to an abnormality of tyrosine hydroxylase gene. This hypothesis has been tested using a cDNA tyrosine hydroxylase gene probe in three families with this disorder. No evidence for genetic linkage between the disease and tyrosine hydroxylase loci was found; it is possible that the disorder results from a post-transcriptional defect confined to the brain.
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