A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17 alpha-hydroxylase deficiency
A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17 alpha-hydroxylase deficiency
复制标题
CYP17A1 基因中独特的外显子剪接突变是类固醇 17 α-羟化酶缺乏的原因
DOI：
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发表时间：
2011
影响因子：
5.8
通讯作者：
Jiang, Bo-Ren
中科院分区：
文献类型：
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作者：
Song, Huai-Dong;Han, Bing;Liu, Bing-Li;Liu, Wei;Wu, Jia-Jun;Pan, Chun-Ming;Jiang, He;Gu, Ting;Jiang, Bo-Ren
