R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease? [electronic resource]

By: Contributor(s): Producer: 20010405Description: 70 p. digitalISSN:
  • 1018-4813
Subject(s): Online resources: In: European journal of human genetics : EJHG vol. 9
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Publication Type: Comment; Letter; Research Support, Non-U.S. Gov't

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