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The fish odour syndrome.

作者信息

Walker V

出版信息

BMJ. 1993 Sep 11;307(6905):639-40. doi: 10.1136/bmj.307.6905.639.

Abstract
摘要

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本文引用的文献

1
Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).
Am J Med Genet. 1993 Feb 1;45(3):335-9. doi: 10.1002/ajmg.1320450310.
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The fish odor syndrome. Trimethylaminuria.
JAMA. 1984 Jan 13;251(2):253-5.
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Trimethylamine N-oxide synthesis: a human variant.
Biochem Med. 1972 Aug;6(4):392-6. doi: 10.1016/0006-2944(72)90025-7.
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Trimethylaminuria: the fish-odour syndrome.
Lancet. 1970 Oct 10;2(7676):770-1. doi: 10.1016/s0140-6736(70)90241-2.
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A genetic polymorphism of the N-oxidation of trimethylamine in humans.
Clin Pharmacol Ther. 1987 Nov;42(5):588-94. doi: 10.1038/clpt.1987.201.
7
Lactulose in trimethylaminuria, the fish-odour syndrome.
Helv Paediatr Acta. 1989 Feb;43(4):345-8.
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Molecular cloning of the flavin-containing monooxygenase (form II) cDNA from adult human liver.
Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1685-9. doi: 10.1073/pnas.89.5.1685.

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