Detection of MYD88 L265P and WHIM-like CXCR4 mutation in patients with IgM monoclonal gammopathy related disease-Reference-Cited by-同舟云学术

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Detection of MYD88 L265P and WHIM-like CXCR4 mutation in patients with IgM monoclonal gammopathy related disease

Published:2017-03-09 Issue:6 Volume:96 Page:971-976
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Cao Xin-xin,Meng Qi,Cai Hao,He Tian-Hua,Zhang Cong-li,Su Wei,Sun Jian,Li Yue,Xu Wei,Zhou Dao-bin,Li Jian

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-017-2968-z.pdf

Reference22 articles.

1. Cao XX, Meng Q, Mao YY et al (2016) The clinical spectrum of IgM monoclonal gammopathy: a single center retrospective study of 377 patients. Leuk Res 46:85–88

2. Treon SP, Xu L, Yang G et al (2012) MYD88 L265P somatic mutation in Waldenström's macroglobulinemia. N Engl J Med 367:826–833

3. Xu L, Hunter ZR, Yang G et al (2013) MYD88 L265P in Waldenstro ̈m macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction. Blood 121:2051–2058

4. Treon SP, Cao Y, Xu L et al (2014) Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenström macroglobulinemia. Blood 123:2791–2796

5. Owen RG, Treon SP, Al-Katib A et al (2003) Clinicopathological definition of Waldenstrom’s macroglobulinemia: consensus panel recommendations from the second international workshop on Waldenstrom’s macroglobulinemia. Semin Oncol 30:110–115

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