A truncating mutation in B3GNT1 causes severe Walker-Warburg syndrome. [electronic resource]

By: Contributor(s): Producer: 20140623Description: 243-5 p. digitalISSN:
  • 1364-6753
Subject(s): Online resources: In: Neurogenetics vol. 14
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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