Novel CYP17A1 mutation in a Japanese patient with combined 17 α-hydroxylase/17,20-lyase deficiency
Autor: | Katsumata, Noriyuki, Ogawa, Eishin, Fujiwara, Ikuma, Fujikura, Kaori |
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Zdroj: | In Metabolism 2010 59(2):275-278 |
Databáze: | ScienceDirect |
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