Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

The monogenic primary dystonias

(2009) U. Muller   BRAIN

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

(2009) F. Clot et al.   BRAIN

Molecular analyses of GCH-1, TH and parkin genes in Chinese dopa-responsive dystonia families

(2009) Z-Y Wu et al.   CLINICAL GENETICS

Tyrosine hydroxylase deficiency with severe clinical course

(2009) D.I. Zafeiriou et al.   MOLECULAR GENETICS AND METABOLISM

Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene

(2009) Diane Doummar et al.   MOVEMENT DISORDERS

Mutations in human monoamine-related neurotransmitter pathway genes

(2008) Jan Haavik et al.   HUMAN MUTATION

Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrations

(2008) M.M. Verbeek et al.   MOLECULAR GENETICS AND METABOLISM