Sequence variations in the flavin-containing mono-oxygenase 3 gene (FMO3) in fish odour syndrome
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.1999.02693.x/fullpdf
Reference15 articles.
1. Trimethylaminuria (fish-odour syndrome): an inborn error of oxidative metabolism;al-Waiz;Lancet,1987
2. Trimethylaminuria (‘fish-odour syndrome’): a study of an affected family;al-Waiz;Clin Sci,1988
3. The fish-odour syndrome: biochemical, familial and clinical aspects;Ayesh;Br Med J,1993
4. The fish-odour syndrome;Mitchell;Perspect Biol Med,1996
5. The fish-odor syndrome: trimethylaminuria;Shelley;JAMA,1984
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