Mutations in the Tyrosine Hydroxylase Gene Cause Various Forms of L-Dopa-Responsive Dystonia-Reference-Cited by-同舟云学术

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Mutations in the Tyrosine Hydroxylase Gene Cause Various Forms of L-Dopa-Responsive Dystonia

Published:1997 Issue: Volume: Page:48-49
ISSN:1054-3589
Container-title:Advances in Pharmacology
language:
Short-container-title:

Author:

Bartholomé Klaus,Lüdecke Barbara

Publisher

Elsevier

Reference5 articles.

1. Hereditary progressive dystonia with marked diurnal fluctuation cdused by mutations in the GTP cyclohydrolase I gene;Ichinose;Nat. Genet.,1994

2. A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome;Lüdecke;Hum. Genet.,1995

3. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene;Knappskog;Hum. Mol. Genet.,1995

4. Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene;Lüdecke;Hum. Mol. Genet.,1996

5. Frequent sequence variant in the human tyrosine hydroxylase gene;Lüdecke;Hum. Genet.,1995

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