Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif.
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| Title: | Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif. |
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| Authors: | Rubtsov, Petr1,2, Nizhnik, Alexander3, Dedov, Ivan3, Kalinchenko, Natalia3, Petrov, Vasily3, Orekhova, Anna1,4, Spirin, Pavel3, Prassolov, Vladimir1,2, Tiulpakov, Anatoly3 ant@endocrincentr.ru |
| Source: | European Journal of Endocrinology. May2015, Vol. 172 Issue 5, pK19-K25. 7p. |
| Database: | Academic Search Ultimate |
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