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Article

A novel CYP2C9 variant that caused erroneous genotyping in a patient on warfarin therapy.

Pharmacogenetics - 1 Oct 2004

Okuda Rika, Izumoto Hiromi, Nishiki Masaki, Matsuura Kayo, Matsuzaki Keisuke, Uemichi Tomoyuki, Suzuki Tomokazu

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 15454736
DOI: 10.1097/00008571-200410000-00009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A novel CYP2C9 variant that caused erroneous genotyping in a patient on warfarin therapy.PMID 15454736Read ↗

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Anticoagulation therapy: Warfarin dosing--novel SNP identified.Semantic proximity Read ↗

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC1*2A and the CYP2C9*3/*3 alleles: genetic testing to support switching to new oral anticoagulants.Semantic proximity Read ↗

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