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 (Q73297718)
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scientific article published on March 28, 2003
Language | Label | Description | Also known as |
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English | 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 |
scientific article published on March 28, 2003 |
Statements
A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters (English)
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 (English)
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Jie Qiao
Ren-Ming Hu
Yong-De Peng
Huai-Dong Song
Yi-Wen Peng
Guo-Feng Gao
Jian-Hua Hao
Nan-Ying Hu
Man-Yin Xu
Jia-Lun Chen
1 March 2003
28 March 2003
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