Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif. - Rubtsov, Petr; Nizhnik, Alexander; Dedov, Ivan; Kalinchenko, Natalia; Petrov, Vasily; Orekhova, Anna; Spirin, Pavel; Prassolov, Vladimir; Tiulpakov, Anatoly (European Journal of Endocrinology, 2015)