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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

2013-01-01

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Literature Corpus work: dfeeec82-841f-5248-840b-ad61c0d3be0c
DOI: 10.1186/1687-9856-2013-s1-p128
PMCID: PMC3850078

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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 defficiencyDOI 10.1186/1687-9856-2013-s1-p128Read

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