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Lancet. 1999 Sep 4;354(9181):834-5.
Zschocke J, Kohlmueller D, Quak E, Meissner T, Hoffmann GF, Mayatepek E.
Comment in:
Mild to transient trimethylaminuria is caused by common variants in the FMO3 gene leading to greatly reduced enzyme activity in vivo. FMO3 deficiency may have clinical relevance well beyond unpleasant body odour.
PMID: 10485731 [PubMed - indexed for MEDLINE]
Hum Mutat. 2003 Sep; 22(3):209-13.
[Hum Mutat. 2003]
Chem Res Toxicol. 1997 Aug; 10(8):837-41.
[Chem Res Toxicol. 1997]
Mol Genet Metab. 2006 Jun; 88(2):192-5. Epub 2006 Apr 4.
[Mol Genet Metab. 2006]
Mol Genet Metab. 1999 Sep; 68(1):24-31.
[Mol Genet Metab. 1999]
Mutat Res. 2006 Jun; 612(3):165-71. Epub 2006 Feb 14.
[Mutat Res. 2006]
Hisamuddin IM, Yang VW. Pharmacogenomics. 2007 Jun; 8(6):635-43.
[Pharmacogenomics. 2007]
Shimizu M, Cashman JR, Yamazaki H. BMC Med Genet. 2007 Jan 27; 8:2. Epub 2007 Jan 27.
[BMC Med Genet. 2007]
Dolan C, Shields DC, Stanton A, O'Brien E, Lambert DM, O'Brien JK, Treacy EP. BMC Med Genet. 2005 Dec 2; 6:41. Epub 2005 Dec 2.
[BMC Med Genet. 2005]
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
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Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
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Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
PubChem chemical substance (submitted) records that are classified under the same Medical Subject Headings (MeSH) controlled vocabulary as the current articles.
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