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TPMT3 is the most prevalent mutant allele associated with thiopurine S‐methyltransferase (TPMT) deficiency in caucasians
Author(s) -
Yates Charles R.,
Krynetski Eugene,
Tai HungLiang,
Loennechen Thrina,
Evans William E
Publication year - 1996
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/sj.clpt.1996.288
Subject(s) - thiopurine methyltransferase , clinical pharmacology , allele , medicine , pharmacology , pharmacogenetics , methyltransferase , genetics , biology , azathioprine , genotype , gene , disease , methylation
Clinical Pharmacology & Therapeutics (1996) 59 , 197–197; doi: 10.1038/sj.clpt.1996.288