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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.
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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An: 101879473
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  Data: 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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  Data: <searchLink fieldCode="AR" term="%22Rubtsov%2C+Petr%22">Rubtsov, Petr</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Nizhnik%2C+Alexander%22">Nizhnik, Alexander</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Dedov%2C+Ivan%22">Dedov, Ivan</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Kalinchenko%2C+Natalia%22">Kalinchenko, Natalia</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Petrov%2C+Vasily%22">Petrov, Vasily</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Orekhova%2C+Anna%22">Orekhova, Anna</searchLink><relatesTo>1,4</relatesTo><br /><searchLink fieldCode="AR" term="%22Spirin%2C+Pavel%22">Spirin, Pavel</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Prassolov%2C+Vladimir%22">Prassolov, Vladimir</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Tiulpakov%2C+Anatoly%22">Tiulpakov, Anatoly</searchLink><relatesTo>3</relatesTo><i> ant@endocrincentr.ru</i>
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Endocrinology%22">European Journal of Endocrinology</searchLink>. May2015, Vol. 172 Issue 5, pK19-K25. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=101879473
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        Value: 10.1530/EJE-14-0834
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        Text: English
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        StartPage: K19
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      – TitleFull: 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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              Text: May2015
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              Value: 172
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            – TitleFull: European Journal of Endocrinology
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