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atrial septal defect, with or without av conduction defects
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NKX2-5
Congenital heart disease caused by mutations in the transcription factor NKX2-5
Homeodomain-interacting protein kinases, a novel family of co-repressors for homeodomain transcription factors
Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tisue-specifying homeobox gene product Csx/Nkx2.5
Cancer Gene Census
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