RUNX1:CBFB:PF4 gene

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

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

J. Thromb. Haemost. 2011
Participants
Participant Of
This entity regulates