In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia. [electronic resource]

By: Contributor(s): Producer: 20150903Description: 37-44 p. digitalISSN:
  • 1365-2265
Subject(s): Online resources: In: Clinical endocrinology vol. 82
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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