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Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency

Detalles Bibliográficos
Autores principales:	Dung, Vu Chi, Khanh, Tran Van, Fukami, Maki, Phuong, Le Thi, Ha, Nguyen Thi, Liem, Nguyen Thanh, Van, Ta Thanh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850078/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P128

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