Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism. [electronic resource]

By: Contributor(s): Producer: 20190909Description: 145-147 p. digitalISSN:
  • 1873-5126
Subject(s): Online resources: In: Parkinsonism & related disorders vol. 55
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Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't

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