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Q30443541-F1AA1655-2D35-419B-9B51-8180FAE16653
Q30443541-F1AA1655-2D35-419B-9B51-8180FAE16653
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30443541-F1AA1655-2D35-419B-9B51-8180FAE16653
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
P2860
Q30443541-F1AA1655-2D35-419B-9B51-8180FAE16653
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30443541-F1AA1655-2D35-419B-9B51-8180FAE16653
rank
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Statement
wasDerivedFrom
e70606b27c1737a05711b76d9d7f5482257fc832
P2860
A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.