NUDT15 p.R139C variant is common and strongly associated with azathioprine-induced early leukopenia and severe alopecia in Korean patients with various neurological diseases
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference18 articles.
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1. Azathioprine-related alopecia totalis due to NUDT 15 mutation in a pregnant systemic lupus erythematosus patient with successful obstetric outcome;Rheumatology;2024-08-08
2. Association of <i>NUDT15</i> gene polymorphism with adverse reaction, treatment efficacy, and dose of 6-mercaptopurine in patients with acute lymphoblastic leukemia: a systematic review and meta-analysis;Haematologica;2023-10-05
3. Time to incorporate preemptive NUDT15 testing before starting thiopurines in inflammatory bowel disease in Asia and beyond: a review;Expert Review of Clinical Pharmacology;2023-07-03
4. NUDT15 Genotyping in Thiopurine Drug Therapy;Laboratory Medicine Online;2022-10-01
5. Implementation of NUDT15 Genotyping to Prevent Azathioprine‐Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population;Clinical Pharmacology & Therapeutics;2022-08-22
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