Related Experiment Video
Updated: Jun 20, 2026

Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation
1Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Lower Lane, Fazakerley, Liverpool L9 7LJ, United Kingdom. a.larner@thewaltoncentre.nhs.uk
Abstract:
Two families with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) resulting from the microtubule associated protein tau (MAPT) gene IVS10+16C>T splice site mutation are reported, members of which showed variable clinical phenotypes at presentation. Possible explanations for the intra- and interfamilial clinical heterogeneity associated with this MAPT mutation are discussed.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Animal Mitochondrial Genetics
Point and Frameshift Mutations
Alternative RNA Splicing
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
Microtubule Associated Proteins (MAPs)
Pedigree Analysis
