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Article

Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystonia.

Advances in pharmacology (San Diego, Calif.) - 1 Jan 1998

Bartholomé K, Lüdecke B

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PMID: 9327843
DOI: 10.1016/s1054-3589(08)60692-4

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Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystonia.PMID 9327843Read ↗

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Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.Semantic proximity Read ↗

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Dopa-responsive dystonia.Semantic proximity Read ↗

Tetrahydrobiopterin metabolism and GTP cyclohydrolase I mutations in L-dopa-responsive dystonia.Semantic proximity Read ↗

Biochemical and Molecular Genetic Characteristics of the Severe Form of Tyrosine Hydroxylase DeficiencySemantic proximity Read ↗

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.Semantic proximity Read ↗

Long-term course of l -dopa-responsive dystonia caused by tyrosine hydroxylase deficiencySemantic proximity Read ↗

Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia.Semantic proximity Read ↗

Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutations.Semantic proximity Read ↗

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