Lack of point mutation of the APP gene in sporadic Alzheimer's disease in Japanese. [electronic resource]

By: Contributor(s): Producer: 19961018Description: 138-41 p. digitalISSN:
  • 0001-6314
Subject(s): Online resources: In: Acta neurologica Scandinavica vol. 93
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

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