Is phenotypic variation of hereditary progressive dystonia with marked diurnal fluctuation/dopa-responsive dystonia (HPD/DRD) caused by the difference of the locus of mutation on the GTP cyclohydrolase 1 (GCH-1) gene?

Advances in neurology

Volumn 94, Issue , 2004, Pages 217-223

  Segawa, Masaya ^a   Nomura, Yoshiko ^a   Yukishita, Shoko ^a   Nishiyama, Nobuyoshi ^a   Yokochi, Masayuki ^a  

^a Segawa Neurological Clinic for Children   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE I; LEVODOPA;

ADOLESCENT; ADULT; AGED; ARTICLE; CLASSIFICATION; COMPARATIVE STUDY; DYSTONIA; EXON; FAMILY HEALTH; FEMALE; GENETICS; HUMAN; INTRON; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PEDIGREE; PHENOTYPE;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; DNA MUTATIONAL ANALYSIS; DYSTONIA; EXONS; FAMILY HEALTH; FEMALE; GTP CYCLOHYDROLASE; HUMANS; INTRONS; LEVODOPA; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE;

EID: 0142135443     PISSN: 00913952     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)