MYD88 and CXCR4 Mutation Profiling in Lymphoplasmacytic Lymphoma/Waldenstrom’s Macroglobulinaemia

Recurrent mutations affecting MYD88 and CXCR4 gene nowadays form the basis for the diagnosis, risk stratification and use of inhibitors targeting these signalling pathways in LPL/WM which are rare B cell neoplasms. MYD88 L265P mutation analysis was performed on 33 cases of LPL/WM by AS-PCR (positivi...

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Dades bibliogràfiques
Publicat a:Indian J Hematol Blood Transfus
Autors principals: Vinarkar, Sushant, Arora, Neeraj, Chowdhury, Sourav Sarma, Saha, Kallol, Pal, Biswajoy, Parihar, Mayur, Radhakrishnan, Vivek S., Chakrapani, Anupam, Bhartia, Shilpa, Bhave, Saurabh, Chandy, Mammen, Nair, Reena, Mishra, Deepak Kumar
Format: Artigo
Idioma:Inglês
Publicat: Springer India 2018
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6369099/
https://ncbi.nlm.nih.gov/pubmed/30828149
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-018-0978-1
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