A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature

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Bibliographic Details
Published in:Oman medical journal 2015, Vol.30 (2), p.129-134
Main Authors: Al-Sinani, Aisha, Mula-Abed, Waad-Allah S, Al-Kindi, Manal, Al-Kusaibi, Ghariba, Al-Azkawi, Hanan, Nahavandi, Nahid
Format: Report
Language:English
Online Access:Get full text
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ISSN:1999-768X
DOI:10.5001/omj.2015.27