A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Source
Nature genetics - ISSN 1061-4036-58:4 (2026) p. 726-736
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes
Source
Molecular neurodegeneration - ISSN 1750-1326-20:1 (2025) p. 1-27
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U
Source
Acta neuropathologica - ISSN 1432-0533-150:1 (2025) p. 1-17
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health
Source
Molecular neurodegeneration - ISSN 1750-1326-20:1 (2025) p. 1-26