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Article

Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency.

Clinical endocrinology - 1 Jun 2014

Chu Xiaojing, Ding Hu, Cui Guanglin, Xu Yujun, Wang Dao Wen, He Yebing

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Share to Adrenal Hyperplasia, Congenital
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 23927611
DOI: 10.1111/cen.12309

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