MYD88 L265P Mutations Are Correlated with 6q Deletion in Korean Patients with Waldenström Macroglobulinemia

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 patien...

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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4033400/
https://ncbi.nlm.nih.gov/pubmed/24895570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/363540
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