Associated Papers
Tyrosine hydroxylase deficiency-Clinical insights and a novel deletion in TH gene in an Indian patient.
Bijarnia-Mahay S et al.
Jimd Reports, 2020
Low frequency of GCH1 and TH mutations in Parkinson's disease.
Rengmark A et al.
Parkinsonism & Related Disorders, 2016
Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's disease.
Bademci G et al.
Cns & Neurological Disorders Drug Targets, 2012
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
Bademci G et al.
Human Mutation, 2010
Adrenergic polymorphism and the human stress response.
Rao F et al.
Annals of the New York Academy of Sciences, 2008
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo.
Rao F et al.
Circulation, 2007
Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease.
Hertz JM et al.
European Journal of Neurology, 2006
Select a paper to view details