Dopa-responsive dystonia caused by tyrosine hydroxylase deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference44 articles.
1. Hereditary progressive dystonia with marked diurnal fluctuation;Segawa;Adv Neurol,1976
2. Dopa responsive dystonia;Nygaard;Adv Neurol,1988
3. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease);Segawa;Ann Neurol,2003
4. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene;Ichinose;Nat Genet,1994
5. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene;Knappskog;Hum Mol Genet,1995
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3. Compound heterozygous mutations in three Chinese patients of Segawa syndrome and their treatment outcomes;International Journal of Developmental Neuroscience;2024-04-02
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