Deleterious mutations in the flavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria

Pharmacogenetics

Volumn 13, Issue 8, 2003, Pages 495-500

  Zhang, Jun ^a   Tran, Quyen ^a   Lattard, Virginie ^a   Cashman, John R ^a  

^a HUMAN BIOMOLECULAR RESEARCH INSTITUTE   (United States)

Author keywords

Flavin containing monooxygenase 3; Mutation; Trimethylaminuria

Indexed keywords

ADENINE; DIMETHYLANILINE MONOOXYGENASE; FLAVIN CONTAINING MONOOXYGENASE 3; GLUTAMIC ACID; GUANINE; HYBRID PROTEIN; MALTOSE BINDING PROTEIN; TRIMETHYLAMINE; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; ENZYME ACTIVITY; ESCHERICHIA COLI; EXON; GENE AMPLIFICATION; GENE DELETION; GENE FREQUENCY; GENE MUTATION; HETEROZYGOSITY; HUMAN; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; OXYGENATION; PEDIGREE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TRIMETHYLAMINURIA;

AMINO ACID SEQUENCE; BASE SEQUENCE; DNA PRIMERS; HUMANS; METABOLISM, INBORN ERRORS; METHYLAMINES; MOLECULAR SEQUENCE DATA; MUTATION; OXYGENASES; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID;

ESCHERICHIA COLI;

EID: 0042383168     PISSN: 0960314X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00008571-200308000-00007     Document Type: Article

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