Biochemical and molecular studies in mild flavin monooxygenase 3 deficiency

Journal of Inherited Metabolic Disease

Volumn 23, Issue 4, 2000, Pages 378-382

  Zschocke, J ^a   Mayatepek, E ^a  

^a UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; DIMETHYLANILINE MONOOXYGENASE; TRIMETHYLAMINE;

ALLELE; CASE REPORT; CHROMOSOME 1Q; CLINICAL FEATURE; CONFERENCE PAPER; DNA POLYMORPHISM; ENZYME DEFICIENCY; GAS CHROMATOGRAPHY; GENE MUTATION; HUMAN; MOLECULAR BIOLOGY; ODOR; URINE LEVEL;

ALLELES; CHILD; CHILD, PRESCHOOL; HETEROZYGOTE; HUMANS; INFANT; METHYLAMINES; ODORS; OXYGENASES;

EID: 0034129542     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005647701321     Document Type: Conference Paper

References (13)

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