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Updated: Jan 11, 2026

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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A Novel Rapidly Progressive Parkinsonism Phenotype with Ophthalmoplegia Associated with the APP p.D678H Mutation
Chao-Yu Liu1, Huan-Yun Chen2, Chuo-Yu Lee3,4
1Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
Movement Disorders Clinical Practice
|November 18, 2025
Abstract
No abstract available in PubMed .
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