Associated Papers
Clinical and genetic spectrum of L-dopa responsive dystonia: insights from seven Egyptian cases.
Almenabawy N et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review.
Weissbach A et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2022
Dopa-responsive dystonia caused by tyrosine hydroxylase deficiency: Three cases report and literature review.
Dong HY et al.
Medicine, 2020
Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites.
Long T et al.
Nature Genetics, 2017
Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene.
Verbeek MM et al.
Annals of Neurology, 2007
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