Gestri et al., 2009 - Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators. Human genetics   126(6):791-803 Full text @ Hum. Genet.
3 Genes / Markers
Marker Type Symbol Name
Gene bmp4 bone morphogenetic protein 4
Gene tcf7l1a transcription factor 7 like 1a
Gene tfap2a transcription factor AP-2 alpha