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
Journal of Clinical Pediatrics . 2018, (4): 256 - .  DOI: 10.3969/j.issn.1000-3606.2018.04.005