The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease
Harry V. Vinters, Wim Annaert, Mihaela Campan, Bart De Strooper et al.
Journal
Molecular Neurodegeneration Advances
Topics
Alzheimer's disease research and treatments
article
The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease
Harry V. Vinters, Wim Annaert, Mihaela Campan, Bart De Strooper, Lutgarde Serneels, Lucía Chávez‐Gutiérrez, Shino Magaki, Inmaculada Sanjuan-Ruiz, Joanna C. Jen, David W. Craig, Katleen Craessaerts, John M. Ringman, Nasim Sheikh‐Bahaei, Alison Goate, Yonggang Shi, Eliana Marisa Ramos, Pamela Ward, Kelly Bartlone
article en
Abstract
No abstract available for this paper.
Publication Tag
Molecular Neurodegeneration AdvancesVol. 1(1)
Institutions
University of Southern California (US), City Of Hope National Medical Center (US), University of California, Los Angeles (US), Keck Hospital of USC (US), Vlaams Instituut voor Biotechnologie (BE), Alzheimer’s Disease Neuroimaging Initiative (US), UK Dementia Research Institute (GB), VIB-KU Leuven Center for Brain & Disease Research (BE), University College London (GB), Icahn School of Medicine at Mount Sinai (US)
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The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease — Harry V. Vinters, Wim Annaert, et al. · Molecular Neurodegeneration Advances (2025) | TGRS Research Map | TGRS