Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency
LHX3基因杂合突变可能导致轻度垂体激素联合缺乏症表型。
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-018-0264-6
Jullien, Nicolas; Romanet, Pauline; Philippon, Mélanie; Quentien, Marie-Hélène; Beck-Peccoz, Paolo; Bergada, Ignacio; Odent, Sylvie; Reynaud, Rachel; Barlier, Anne; Saveanu, Alexandru; Brue, Thierry; Castinetti, Frederic