Article
Human flavin-containing monooxygenase form 3: cDNA expression of the enzymes containing amino acid substitutions observed in individuals with trimethylaminuria.
Chemical research in toxicology - 1 Aug 1997
Cashman J R, Bi Y A, Lin J, Youil R, Knight M, Forrest S, Treacy E
Abstract excerpt
Trimethylaminuria is an autosomal recessive human disorder affecting a small part of the population as an inherited polymorphism. Individuals diagnosed with trimethylaminuria excrete relatively large amounts of trimethylamine in their urine, sweat, and breath, and this results in a fishy odor cha...
Topics
- DNA, Complementary
- Humans
- Metabolism, Inborn Errors
- Methylamines
- Mutation
- Odorants
- Oxygenases
- Structure-Activity Relationship
