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Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

14 Apr 2019

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PMID: 30995443
DOI: 10.1016/j.clinbiochem.2019.04.008

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Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyPMID 30995443Read ↗

Genetic analysis and novel variation identification in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.Semantic proximity Read ↗

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Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.Semantic proximity Read ↗

Molecular characterization of 25 Chinese pedigrees with 21-hydroxylase deficiency.Semantic proximity Read ↗

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