Molecular mechanisms of glycine transporter GlyT2 mutations in startle disease. [electronic resource]

By: Contributor(s): Producer: 20121212Description: 283-9 p. digitalISSN:
  • 1437-4315
Subject(s): Online resources: In: Biological chemistry vol. 393
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

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