Mutations in the flavin-containing monooxygenase form 3 (FMO3) gene cause trimethylaminuria, fish odour syndrome.

被引:0
|
作者
Akerman, BR
Chow, L
Forrest, S
Youil, R
Cashman, J
Treacy, EP
机构
[1] McGill Univ, Montreal Childrens Hosp, Res Inst, Montreal, PQ H3H 1P3, Canada
[2] Royal Childrens Hosp, Murdoch Inst, Melbourne, Vic, Australia
[3] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[4] Merck Res Labs, W Point, PA USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
281
引用
收藏
页码:A53 / A53
页数:1
相关论文
共 50 条
  • [1] Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication
    Treacy, EP
    Akerman, BR
    Chow, LML
    Youil, R
    Bibeau, C
    Lin, J
    Bruce, AG
    Knight, M
    Danks, DM
    Cashman, JR
    Forrest, SM
    HUMAN MOLECULAR GENETICS, 1998, 7 (05) : 839 - 845
  • [2] Deleterious mutations in the flavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria
    Zhang, J
    Tran, Q
    Lattard, V
    Cashman, JR
    PHARMACOGENETICS, 2003, 13 (08): : 495 - 500
  • [3] Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FMO3) gene in patients with fish-odour syndrome
    Dolphin, CT
    Janmohamed, A
    Smith, RL
    Shephard, EA
    Phillips, IR
    PHARMACOGENETICS, 2000, 10 (09): : 799 - 807
  • [4] Stop codon mutations in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population
    Yamazaki, Hiroshi
    Fujita, Haruka
    Gunji, Takaaki
    Zhang, Jun
    Kamataki, Tetsuya
    Cashman, John R.
    Shimizu, Makiko
    MOLECULAR GENETICS AND METABOLISM, 2007, 90 (01) : 58 - 63
  • [5] Novel variants of the human flavin-containing monooxygenase 3 (FMO3) gene associated with trimethylaminuria
    Motika, Meike S.
    Zhang, Jun
    Zheng, Xueying
    Riedler, Kiersten
    Cashman, John R.
    MOLECULAR GENETICS AND METABOLISM, 2009, 97 (02) : 128 - 135
  • [6] Variants in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population
    Shimizu, Makiko
    Kobayashi, Yuko
    Hayashi, Shoko
    Aoki, Yuka
    Yamazaki, Hiroshi
    MOLECULAR GENETICS AND METABOLISM, 2012, 107 (03) : 330 - 334
  • [7] A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria
    Forrest, SM
    Knight, M
    Akerman, BR
    Cashman, JR
    Treacy, EP
    PHARMACOGENETICS, 2001, 11 (02): : 169 - 174
  • [8] MUTATIONS OF FLAVIN-CONTAINING MONOOXYGENASE 3 (FMO3) GENE IN JAPANESE COHORTS
    Shimizu, Makiko
    Nakakuki, Komei
    Yoda, Hiromi
    Hiratsuka, Masahiro
    Yamazaki, Hiroshi
    DRUG METABOLISM AND PHARMACOKINETICS, 2019, 34 (01) : S63 - S63
  • [9] Biochemical and clinical aspects of the human flavin-containing monooxygenase form 3 (FMO3) related to trimethylaminuria
    Cashman, JR
    Camp, K
    Fakharzadeh, SS
    Fennessey, PV
    Hines, RN
    Mamer, OA
    Mitchell, SC
    Preti, G
    Schlenk, D
    Smith, RL
    Tjoa, SS
    Williams, DE
    Yannicelli, S
    CURRENT DRUG METABOLISM, 2003, 4 (02) : 151 - 170
  • [10] A novel mutation in the flavin-containing monooxygenase 3 gene (FMO3) of a Norwegian family causes trimethylaminuria
    Allerston, C. K.
    Vetti, H. H.
    Houge, G.
    Phillips, I. R.
    Shephard, E. A.
    MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 198 - 202