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24. Partial deficiency of 17α-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif. Rubtsov P; Nizhnik A; Dedov I; Kalinchenko N; Petrov V; Orekhova A; Spirin P; Prassolov V; Tiulpakov A Eur J Endocrinol; 2015 May; 172(5):K19-25. PubMed ID: 25650406 [TBL] [Abstract][Full Text] [Related]
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