Genetic defects in PRC2 components other than EZH2 are not common in myeloid malignancies

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Bibliographische Detailangaben
Veröffentlicht in:	Blood 2012-02, Vol.119 (5), p.1318-1319
Hauptverfasser:	Kroeze, Leonie I., Nikoloski, Gorica, da Silva-Coelho, Pedro, van Hoogen, Patricia, Stevens-Linders, Ellen, Kuiper, Roland P., Schnittger, Susanne, Haferlach, Torsten, Pahl, Heike L., van der Reijden, Bert A., Jansen, Joop H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Carrier Proteins - genetics Cohort Studies DNA-Binding Proteins - genetics Enhancer of Zeste Homolog 2 Protein Gene Frequency Genetic Predisposition to Disease Genetic Variation - physiology Hematologic Neoplasms - genetics Humans Myelodysplastic Syndromes - genetics Myeloproliferative Disorders - genetics Nuclear Proteins - genetics Polycomb Repressive Complex 2 Polycomb-Group Proteins Polymorphism, Single Nucleotide Repressor Proteins - genetics Transcription Factors - genetics
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