A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome. [electronic resource]

By: Contributor(s): Producer: 20110427Description: 197-9 p. digitalISSN:
  • 1365-2133
Subject(s): Online resources: In: The British journal of dermatology vol. 164
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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