RUNX1:CBFB:PF4 gene [nucleoplasm]

Stable Identifier
R-HSA-8938178
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
21129147 Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4

Rao, AK, Singh, A, Jalagadugula, G, Mao, G, Aneja, K

J. Thromb. Haemost. 2011
Participants
Participates
This entity regulates
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