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Mutation spectrum ofCYP21A2and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency
Dung, Vu, Khanh, Tran, Fukami, Maki, Phuong, Le, Ha, Nguyen, Liem, Nguyen, Van, TaVolume:
2013
Language:
english
Journal:
International Journal of Pediatric Endocrinology
DOI:
10.1186/1687-9856-2013-S1-P128
Date:
October, 2013
File:
PDF, 337 KB
english, 2013