[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]. [electronic resource]

By: Contributor(s): Producer: 20090122Description: 1385-91 p. digitalISSN:
  • 0016-6758
Subject(s): In: Genetika vol. 44
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Publication Type: English Abstract; Journal Article; Research Support, Non-U.S. Gov't

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