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.
6 Genes / Markers
Marker Type Symbol Name
Gene sox2 SRY-box transcription factor 2
Gene sox10 SRY-box transcription factor 10
Gene stub1 STIP1 homology and U-Box containing protein 1
Gene tcf3a transcription factor 3a
Gene tcf3b transcription factor 3b
Gene tcf12 transcription factor 12