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This page is a summary of: Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling, Arquivos Brasileiros de Endocrinologia & Metabologia, November 2008, FapUNIFESP (SciELO),
DOI: 10.1590/s0004-27302008000800018.
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