A novel de novo RNF216 mutation associated with autosomal recessive Huntington-like disorder. [electronic resource]

By: Contributor(s): Producer: 20210419Description: 860-864 p. digitalISSN:
  • 2328-9503
Subject(s): Online resources: In: Annals of clinical and translational neurology vol. 7
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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