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 / Model Data (2 Records)
Human Disease Fish Environment Evidence Code
hypogonadotropic hypogonadism
Kallmann syndrome