New England Journal of Medicine· 2012Q1
MYD88 L265P Somatic Mutation in Waldenström's Macroglobulinemia
- 1,281citations
- Q1SCImago
- 2012year
Short summary
The MYD88 L265P somatic mutation is present in 91% of Waldenström's macroglobulinemia (WM) and non-IgM LPL patients, and absent in healthy donors and other B-cell disorders, serving as a diagnostic marker.
AI-generated from the title and abstract; the full text is not read.
TakeawaysIn the app
Key pointsIn the app
Ask the paperIn the app
The rest is in the Pofolia app
Takeaways, key points and questions to the paper; new summaries every day for your field. Free.
Sign in on the web to openField: Genetics
GeneticsMedicine