A severe neurodevelopmental syndrome linked to a South Asian founder variant in the UFMylation adaptor CDK5RAP3

Acta Neuropathologica · Published 2026-04-27 · DOI 10.1007/s00401-026-03017-2

Authors being retrieved — see the publisher record. https://doi.org/10.1007/s00401-026-03017-2

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year: 2026

Related articles

A distinct tau oligomer strain defines the molecular and proteomic landscape of rapidly progressive Alzheimer’s disease · Acta Neuropathologica · 2026 · Same journal
Retinal proteome changes mirror brain pathology and reveal synaptic and cytoskeletal dysfunction in Alzheimer’s disease · Acta Neuropathologica · 2026 · Same journal
Molecular signatures and biomarker development for limbic-predominant age-related TDP-43 encephalopathy (LATE) · Acta Neuropathologica · 2026 · Same journal
APOE ε4 influences the widespread TDP-43 pathological subtype in sporadic amyotrophic lateral sclerosis · Acta Neuropathologica · 2026 · Same journal
Neocortical tau burden determines the degree of cognitive impairment in individuals with Braak stage V neurofibrillary degeneration · Acta Neuropathologica · 2026 · Same journal
Consensus statement on microglial and macrophage functions in gliomas · Acta Neuropathologica · 2026 · Same journal
Prion-like transmission and propagation of human β-amyloid to the bank vole rodent model · Acta Neuropathologica · 2026 · Same journal
Altered astrocyte–neuron crosstalk in progressive supranuclear palsy: integrated evidence from proteomics and magnetic resonance spectroscopy · Acta Neuropathologica · 2026 · Same journal
CTE-type tau filaments in Alzheimer’s disease with co-morbid LATE-NC · Acta Neuropathologica · 2026 · Same journal
A novel BEND2 monoclonal antibody enables highly specific immunohistochemical diagnosis of BEND2-fusion astroblastomas · Acta Neuropathologica · 2026 · Same journal