Alsin Related Disorders: Literature Review and Case Study with Novel Mutations

by Filipa Flor-de-Lima, Mafalda Sampaio, Nahid Nahavandi, Susana Fernandes, Miguel Leão
Published 2014-01-01

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

by Aisha Al-Sinani, Waad-Allah S. Mula-Abed, Manal Al-Kindi, Ghariba Al-Kusaibi, Hanan Al-Azkawi, Nahid Nahavandi
Published 2015-03-01