A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy
Article in Frontiers in Neurology (April 2024)
The most recent citing publications are shown below. View all 25 publications that cite this research output on Dimensions.
Detecting and Validating MAPT Mutations in Neurodegeneration Patients and Analysis of Exon Splicing Consequences
Book chapter (March 2024)
Rare Copy Number Variant analysis in case-control studies using SNP Array Data: a scalable and automated data analysis pipeline
Preprint in bioRxiv (March 2024)