Gene: TH ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7054
Gene Symbol: TH
TH 		0.110 CausalMutation group CLINVAR What is new for monoamine neurotransmitter disorders? 24696406 2014
Entrez Id: 7054
Gene Symbol: TH
TH 		0.110 CausalMutation group CLINVAR Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency. 20823027 2011
Entrez Id: 7054
Gene Symbol: TH
TH 		0.110 CausalMutation group CLINVAR Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. 20430833 2010
Entrez Id: 7054
Gene Symbol: TH
TH 		0.110 GeneticVariation group BEFREE A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder. 11281275 2000