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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The fish odour syndrome.鱼腥味综合征
BMJ. 1993 Sep 11;307(6905):639-40. doi: 10.1136/bmj.307.6905.639.
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Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).一名患有普拉德-威利综合征及15号染色体长臂1区1带至1区3带缺失（del(15)(q11q13)）的女孩出现的三甲胺尿症
Am J Med Genet. 1993 Feb 1;45(3):335-9. doi: 10.1002/ajmg.1320450310.
2
The fish odour syndrome: biochemical, familial, and clinical aspects.鱼腥味综合征：生化、家族性及临床方面
BMJ. 1993 Sep 11;307(6905):655-7. doi: 10.1136/bmj.307.6905.655.
3
The fish odor syndrome. Trimethylaminuria.
JAMA. 1984 Jan 13;251(2):253-5.
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Trimethylamine N-oxide synthesis: a human variant.三甲胺N-氧化物合成：一种人类变体。
Biochem Med. 1972 Aug;6(4):392-6. doi: 10.1016/0006-2944(72)90025-7.
5
Trimethylaminuria: the fish-odour syndrome.
Lancet. 1970 Oct 10;2(7676):770-1. doi: 10.1016/s0140-6736(70)90241-2.
6
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.
8
Flavin-containing monooxygenases: enzymes adapted for multisubstrate specificity.含黄素单加氧酶：适应多底物特异性的酶。
Trends Pharmacol Sci. 1990 Aug;11(8):321-4. doi: 10.1016/0165-6147(90)90235-z.
9
Cloning, primary sequence, and chromosomal mapping of a human flavin-containing monooxygenase (FMO1).
J Biol Chem. 1991 Jul 5;266(19):12379-85.
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Molecular cloning of the flavin-containing monooxygenase (form II) cDNA from adult human liver.成人肝脏中含黄素单加氧酶（II型）cDNA的分子克隆
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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