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.
Marker Type | Symbol | Name |
---|---|---|
Gene | bmp4 | bone morphogenetic protein 4 |
Gene | tcf7l1a | transcription factor 7 like 1a |
Gene | tfap2a | transcription factor AP-2 alpha |