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Thiopurine S-methyltransferase deficiency associated with a novel mutation.

Inflammatory bowel diseases - 1 Nov 2010

Torres Joana, Cortot Antoine, Tremblay Lydjie, Colombel Jean-Fréderic, Jouet Jean-Pierre, Allorge Delphine, Broly Frank

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PMID: 20186941
DOI: 10.1002/ibd.21232

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Identification of a novel thiopurine S-methyltransferase allele (TPMT*37).Semantic proximity Read ↗

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Genetic Polymorphism of Thiopurine S-Methyltransferase: Molecular Mechanisms and Clinical ImportanceSemantic proximity Read ↗

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