Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome. [electronic resource]

By: Contributor(s): Producer: 20080410Description: 1281-4 p. digitalISSN:
  • 0007-0963
Subject(s): Online resources: In: The British journal of dermatology vol. 157
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Publication Type: Letter; Research Support, Non-U.S. Gov't

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