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ID: 1048 A novel nonsense mutation in the CYP21A2 gene of a Vietnamese patient with congenital adrenal hyperplasia

S 129 2017-09-05

Vu Chi Dung, Ngoc Lan Nguyen, Huy Hoang Nguyen, Thi Kim Lien Nguyen, Thinh Huy Tran, Thanh Van Ta, Van Khanh Tran

Evaluating IFN-γ ELISpot in a pediatric case: Unraveling X-linked leaky severe combined immunodeficiency and Omenn syndrome

8215-8221 2026-01-31

Noor Faralina Zainul Fadziruddin, Adli Ali, Intan Juliana Abd Hamid, Zarina Thasneem Zainudeen

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