携带 I2G 突变的 21 羟化酶缺乏症患儿基因突变谱与临床表型的关系

王会贞,　卫海燕,　沈凌花,　杨海花,　陈永兴,　毋盛楠,　王小红

Analysis of the relationship between gene mutation spectrum and clinical phenotype in 21 hydroxylase deficiency with I2G mutation in children

　WANG Huizhen, WEI Haiyan, SHEN Linghua, YANG Haihua, CHEN Yongxing, WU Shengnan, WANG Xiaohong

临床儿科杂志 . 2018, (4): 256 - . DOI: 10.3969/j.issn.1000-3606.2018.04.005