Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1997 | 2 |
1998 | 1 |
2000 | 1 |
2006 | 1 |
2007 | 1 |
2020 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.
Hum Mol Genet. 1998 May;7(5):839-45. doi: 10.1093/hmg/7.5.839.
Hum Mol Genet. 1998.
PMID: 9536088
Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome.
Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.
Dolphin CT, et al.
Pharmacogenetics. 2000 Dec;10(9):799-807. doi: 10.1097/00008571-200012000-00005.
Pharmacogenetics. 2000.
PMID: 11191884
Item in Clipboard
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.
Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA.
Chalmers RA, et al.
J Inherit Metab Dis. 2006 Feb;29(1):162-72. doi: 10.1007/s10545-006-0158-6.
J Inherit Metab Dis. 2006.
PMID: 16601883
Clinical Trial.
Item in Clipboard
Human flavin-containing monooxygenase form 3: cDNA expression of the enzymes containing amino acid substitutions observed in individuals with trimethylaminuria.
Cashman JR, Bi YA, Lin J, Youil R, Knight M, Forrest S, Treacy E.
Cashman JR, et al.
Chem Res Toxicol. 1997 Aug;10(8):837-41. doi: 10.1021/tx9700533.
Chem Res Toxicol. 1997.
PMID: 9282831
Item in Clipboard
Primary Trimethylaminuria.
Phillips IR, Shephard EA.
Phillips IR, et al.
2007 Oct 8 [updated 2020 Nov 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
2007 Oct 8 [updated 2020 Nov 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 20301282
Free Books & Documents.
Review.
Item in Clipboard
Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome.
Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.
Dolphin CT, et al.
Nat Genet. 1997 Dec;17(4):491-4. doi: 10.1038/ng1297-491.
Nat Genet. 1997.
PMID: 9398858
Item in Clipboard
Cite
Cite