Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss. [electronic resource]

By: Contributor(s): Producer: 20050913Description: 161-6 p. digitalISSN:
  • 0009-9163
Subject(s): Online resources: In: Clinical genetics vol. 68
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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