Trimethylaminuria
Publisher
Springer New York
Reference36 articles.
1. Akerman, B. R., Forrest, S., Chow, L., et al. (1999a). Two novel mutations of the FMO3 gene in a proband with trimethylaminuria. Human Mutation, 13, 376–379. 2. Akerman, B. R., Lemass, H., Chow, L., et al. (1999b). Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort. Molecular Genetics and Metabolism, 68, 24–31. 3. Al-Waiz, M., Ayesh, R., Mitchell, S. C., et al. (1987a). Trimethylaminuria (fish-odour syndrome): An inborn error of oxidative metabolism. Lancet, 1, 634–635. 4. Al-Waiz, M., Ayesh, R., Mitchell, S. C., et al. (1987b). A genetic polymorphism of the N-oxidation of trimethylamine in humans. Clinical Pharmacology and Therapeutics, 42, 588–594. 5. Al-Waiz, M., Ayesh, R., Mitchell, S. C., et al. (1988). Trimethylaminuria (“fish-odour syndrome”): A study of an affected family. Clinical Science, 74, 231–236.
|
|