Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
CHD7基因编码一种染色质重塑蛋白,该基因突变会导致特发性低促性腺激素性性腺功能减退症和卡尔曼综合征。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2008.09.005
Kim, Hyung-Goo; Kurth, Ingo; Lan, Fei; Meliciani, Irene; Wenzel, Wolfgang; Eom, Soo Hyun; Kang, Gil Bu; Rosenberger, Georg; Tekin, Mustafa; Ozata, Metin; Bick, David P; Sherins, Richard J; Walker, Steven L; Shi, Yang; Gusella, James F; Layman, Lawrence C