Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency

Journal of Biological Chemistry

Volumn 270, Issue 17, 1995, Pages 10062-10071

  Ichinose, H ^a   Ohye, T ^a   Matsuda, Y ^a   Hori, T A ^a   Blau, N ^a   Burlina, A ^a   Rouse, B ^a   Matalon, R ^a   Fujita, K ^a   Nagatsu, T ^a  

^a FUJITA HEALTH UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

5 HYDROXYTRYPTOPHAN; CARBIDOPA PLUS LEVODOPA; DNA; GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE I; MESSENGER RNA; PHENYLALANINE; PTERIN DERIVATIVE; TETRAHYDROBIOPTERIN;

ANIMAL TISSUE; ARTICLE; CASE REPORT; CHILD; CHOREOATHETOSIS; CHROMOSOME 14; CHROMOSOME MAP; CONTROLLED STUDY; DNA SEQUENCE; DYSTONIA; ENZYME DEFICIENCY; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HUMAN; HUMAN TISSUE; HYPERPHENYLALANINEMIA; INTRON; MOUSE; NONHUMAN; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS; TRANSCRIPTION INITIATION;

AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CHROMOSOME MAPPING; CLONING, MOLECULAR; DNA; DYSTONIA; ESCHERICHIA COLI; GTP CYCLOHYDROLASE; HUMAN; MICE; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID HYBRIDIZATION; SEQUENCE HOMOLOGY, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T; TRANSCRIPTION, GENETIC;

EID: 0028902943     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.270.17.10062     Document Type: Article

References (0)