Molecular genetics of tyrosine 3-monooxygenase and inherited diseases

Biochemical and Biophysical Research Communications

Volumn 338, Issue 1, 2005, Pages 267-270

  Kobayashi, Kazuto ^a   Nagatsu, Toshiharu ^b  

^a FUKUSHIMA MEDICAL UNIVERSITY   (Japan)

^b FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Catecholamine; Dopamine; Dystonia; Encephalopathy; Knockout mouse; Noradrenaline; Parkinsonism; Tyrosine 3 monooxygenase

Indexed keywords

DOPAMINE; LEVODOPA; TYROSINE 3 MONOOXYGENASE;

BRAIN DISEASE; CATALYSIS; CATALYST; CATECHOLAMINE SYNTHESIS; DYSTONIA; ENZYME ACTIVITY; GENE MUTATION; HETEROZYGOSITY; INHERITANCE; INSTRUMENTAL CONDITIONING; KNOCKOUT MOUSE; MOLECULAR GENETICS; MOTOR CONTROL; NEUROPSYCHOLOGICAL TEST; NONHUMAN; PARKINSONISM; POINT MUTATION; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW;

ANIMALS; DISEASE MODELS, ANIMAL; GENETIC DISEASES, INBORN; HUMANS; TYROSINE 3-MONOOXYGENASE;

EID: 27544491345     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2005.07.186     Document Type: Review

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