A complex heterozygous mutation of His373Leu and Asp487–Ser488–Phe489 deletion in human cytochrome P450c17 causes 17α-hydroxylase/17,20-lyase deficiency in three Chinese sisters

Autor: Qiao, Jie, Hu, Ren-Ming, Peng, Yong-De, Song, Huai-Dong, Peng, Yi-Wen, Gao, Guo-Feng, Hao, Jian-Hua, Hu, Nan-Ying, Xu, Man-Yin, Chen, Jia-Lun *
Zdroj: In Molecular and Cellular Endocrinology 2003 201(1):189-195
Databáze: ScienceDirect
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