Waldenström's macroglobulinemia causes: Difference between revisions
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{{Waldenström's macroglobulinemia}} | {{Waldenström's macroglobulinemia}} | ||
The most common causes of Waldenström's macroglobulinemia is somatic mutation in MYD88 (90% of patients) and a somatic mutation in CXCR4 (27% of patients).<ref name="wiki"/> | |||
==References== | ==References== | ||
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[[Category:Hematology]] | [[Category:Hematology]] | ||
Revision as of 15:23, 6 November 2015
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Waldenström's macroglobulinemia Microchapters |
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Differentiating Waldenström's macroglobulinemia from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Waldenström's macroglobulinemia causes On the Web |
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American Roentgen Ray Society Images of Waldenström's macroglobulinemia causes |
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Directions to Hospitals Treating Waldenström's macroglobulinemia |
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Risk calculators and risk factors for Waldenström's macroglobulinemia causes |
The most common causes of Waldenström's macroglobulinemia is somatic mutation in MYD88 (90% of patients) and a somatic mutation in CXCR4 (27% of patients).[1]
References
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