Associated Papers
A single-cell, long-read, isoform-resolved case-control study of FTD reveals cell-type-specific and broad splicing dysregulation in human brain.
Belchikov N et al.
Cell Reports, 2025
40913764 (PubMed )
Supplement: NIHMS2110306-supplement-Supplementary_Information.pdf
Two novel variants in GRN: the relevance of CNV analysis and genetic screening in FTLD patients with a negative family history.
De Houwer JFH et al.
Journal of Neurology, 2024
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