A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase...

Oman Medical Journal 2015 / 3 Vol. 30; Iss. 2

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

Al-Sinani, Aisha, Mula-Abed, Waad-Allah, Al-Kindi, Manal, Al-Kusaibi, Ghariba, Al-Azkawi, Hanan, Nahavandi, Nahid
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Volume:
30
Language:
english
Journal:
Oman Medical Journal
DOI:
10.5001/omj.2015.27
Date:
March, 2015
File:
PDF, 906 KB
english, 2015
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