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[期刊论文] 作者：Na Xi,Xiao Song,Xue-Yan Wang,Sheng-Fang Qin,Guan-Nan He,Ling-Ling Sun,Xi-Min Chen,
来源：世界临床病例杂志 年份：2021
BACKGROUND CYP21A2 gene mutations may all cause reduction or loss of 21-hydroxylase activity,leading to development of congenital adrenal hyperplasia(CAH)with different clinical phenotypes.For families with CAH children,genetic testing of t......
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