Associated Papers
Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.
Fossbakk A et al.
Human Mutation, 2014
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
Willemsen MA et al.
Brain : a Journal of Neurology, 2010
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.
Mak CM et al.
Molecular Genetics and Metabolism, 2010
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease.
Yeung WL et al.
Brain & Development, 2006
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