Article info
Rare disease
Case report
Combined homozygous 21 hydroxylase with heterozygous P450 oxidoreductase mutation in a Saudi boy presented with hypertension
- Correspondence to Dr Aida Aljabri; dr_aida_s{at}hotmail.com
Citation
Combined homozygous 21 hydroxylase with heterozygous P450 oxidoreductase mutation in a Saudi boy presented with hypertension
Publication history
- Accepted August 12, 2020
- First published September 29, 2020.
Online issue publication
September 29, 2020
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© BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.