Davis et al., 2020
- TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci.
Human molecular genetics
29(14):2435-2450
Full text @ Hum. Mol. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | sox10 | SRY-box transcription factor 10 |
| Gene | sox2 | SRY-box transcription factor 2 |
| Gene | stub1 | STIP1 homology and U-Box containing protein 1 |
| Gene | tcf12 | transcription factor 12 |
| Gene | tcf3a | transcription factor 3a |
| Gene | tcf3b | transcription factor 3b |