Nucleophosmin mutations of exon 12 (NPM1 mutations) represent the most frequent molecular aberration that can be found in patients with acute myeloid leukaemia (AML) and can be detected in about 35% of AML patients. NPM1 mutations are characterised by four basepair insertions within the region corre
β¦ LIBER β¦
Rapid and sensitive screening for CEBPA mutations in acute myeloid leukaemia
β Scribed by Tobias Benthaus; Friederike Schneider; Gudrun Mellert; Evelyn Zellmeier; Stephanie Schneider; Purvi M. Kakadia; Wolfgang Hiddemann; Stefan K. Bohlander; Michaela Feuring-Buske; Jan Braess; Karsten Spiekermann; Annika Dufour
- Book ID
- 108675940
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 318 KB
- Volume
- 143
- Category
- Article
- ISSN
- 0007-1048
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