Identification of rare defective allelic variants in cases of thiopurine S-methyltransferase deficient activity
Author:
Affiliation:
1. Service de Biochimie, Assistance Publique Hôpitaux de Paris, Hôpital Européen Georges Pompidou, F-75015, Paris, France
2. Université de Paris, INSERM U1138, Centre de Recherche des Cordeliers, F-75006, Paris, France
Abstract
Publisher
Future Medicine Ltd
Subject
Pharmacology,Genetics,Molecular Medicine
Link
https://www.futuremedicine.com/doi/pdf/10.2217/pgs-2020-0124
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