Results
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43801.
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A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. [electronic resource] by
- Brooke, A M
- Taylor, N F
- Shepherd, J H
- Gore, M E
- Ahmad, T
- Lin, L
- Rumsby, G
- Papari-Zareei, M
- Auchus, R J
- Achermann, J C
- Monson, J P
Producer: 20060629
In:
The Journal of clinical endocrinology and metabolism vol. 91
Availability: No items available.
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