A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17α-hydroxylase deficiency
2006 ◽
Vol 249
(1-2)
◽
pp. 16-20
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1998 ◽
Vol 83
(1)
◽
pp. 199-202
◽
1998 ◽
Vol 83
(1)
◽
pp. 199-202
2020 ◽
Vol 42
(3)
◽
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