Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer’s disease

INTRODUCTION: A minority of patients with sporadic early-onset Alzheimer’s disease (AD) exhibit de novo germ line mutations in the autosomal dominant genes such as APP, PSEN1, or PSEN2. We hypothesized that negatively screened patients may harbor somatic variants in these genes. METHODS: We applied...

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Detalles Bibliográficos
Autores principales: Nicolas, Gaël, Acuña-Hidalgo, Rocío, Keogh, Michael J., Quenez, Olivier, Steehouwer, Marloes, Lelieveld, Stefan, Rousseau, Stéphane, Richard, Anne-Claire, Oud, Manon S., Marguet, Florent, Laquerrière, Annie, Morris, Chris M., Attems, Johannes, Smith, Colin, Ansorge, Olaf, Al Sarraj, Safa, Frebourg, Thierry, Campion, Dominique, Hannequin, Didier, Wallon, David, Gilissen, Christian, Chinnery, Patrick F., Veltman, Joris A., Hoischen, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544509/
https://www.ncbi.nlm.nih.gov/pubmed/30114415
http://dx.doi.org/10.1016/j.jalz.2018.06.3056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544509/
https://www.ncbi.nlm.nih.gov/pubmed/30114415
http://dx.doi.org/10.1016/j.jalz.2018.06.3056

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