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.
Human Disease | Fish | Environment | Evidence Code |
---|---|---|---|
hypogonadotropic hypogonadism | |||
Kallmann syndrome |