Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency.
Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency.
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人细胞色素 P-450(17 α) N 末端区域苯丙氨酸的缺失会导致 17 α-羟化酶/17,20-裂解酶的部分组合缺陷。
DOI：
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发表时间：
1989
期刊：
影响因子：
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通讯作者：
Waterman,MR
中科院分区：
文献类型：
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作者：
Yanase,T;Kagimoto,M;Suzuki,S;Hashiba,K;Simpson,ER;Waterman,MR
