Molecular dissection and anatomical basis of dystonia: X-linked recessive dystonia-parkinsonism (DYT3)

Journal of Medical Investigation

Volumn 52, Issue SUPPL., 2005, Pages 280-283

  Kaji, Ryuji ^a   Goto, Satoshi ^b   Tamiya, Gen ^a   Ando, Satoshi ^a   Makino, Satoshi ^a   Lee, L V ^c  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

^b KUMAMOTO UNIVERSITY   (Japan)

^c Philippines National Children's Medical Center   (Philippines)

Author keywords

Dopamine; Dystonia; DYT3; Striosome; TAF1

Indexed keywords

TRANSCRIPTION FACTOR;

CLINICAL FEATURE; CONFERENCE PAPER; CORPUS STRIATUM; DOPAMINERGIC NERVE CELL; DRD2 GENE; DYSTONIA; GABAERGIC SYSTEM; GENE; GENE EXPRESSION; HUMAN; HUNTINGTON CHOREA; HYPERKINESIA; PARKINSONISM; PATHOLOGY; PHILIPPINES; TAF1 GENE; X LINKED RECESSIVE DYSTONIA PARKINSONISM;

CHROMOSOMES, HUMAN, X; CORPUS STRIATUM; DYSTONIA; GENES, RECESSIVE; GENETIC DISEASES, X-LINKED; HUMANS; MODELS, BIOLOGICAL; NEURONS; PARKINSONIAN DISORDERS; TATA-BINDING PROTEIN ASSOCIATED FACTORS; TRANSCRIPTION FACTOR TFIID;

EID: 30144434480     PISSN: 13431420     EISSN: None     Source Type: Journal    
DOI: 10.2152/jmi.52.280     Document Type: Conference Paper

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