Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference38 articles.
1. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
2. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia- parkinsonism-amyotrophy complex
3. Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21
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