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

By: Contributor(s): Producer: 20190610Description: 44-49 p. digitalISSN:
  • 1873-2933
Subject(s): Online resources: In: Clinical biochemistry vol. 68
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Publication Type: Journal Article

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