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Article

MYD88 L265P mutations are correlated with 6q deletion in Korean patients with Waldenström macroglobulinemia.

BioMed research international - 1 Jan 2014

Kim Jung-Ah, Im Kyongok, Park Si Nae, Kwon Jiseok, Choi Qute, Hwang Sang Mee, Sekiguchi Naohiro, Yoon Sung-Soo, Lee Dong Soon, Kim Seon Young

Abstract excerpt

Waldenström macroglobulinemia (WM) is a malignant lymphoplasma-proliferative disorder with IgM monoclonal gammopathy. A recent whole-genome study identified MYD88 L265P as the key mutation in WM. We investigated MYD88 mutations in conjunction with cytogenetic study in 22 consecutive Korean WM patients. Conventional G-banding and interphase fluorescence in situ hybridization (FISH) were performed at regions...

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Source

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Identifiers

PMID: 24895570
DOI: 10.1155/2014/363540
PMCID: PMC4033400

Genes

MYD88
IGH

Variants

Provenance

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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