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A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site

Crossref DOI link: https://doi.org/10.1038/s41439-021-00160-y

Published Online: 2021-07-21

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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