Mutation analysis of disease causing genes in patients with early onset or familial forms of Alzheimer’s disease and frontotemporal dementia

BACKGROUND: Most dementia disorders have a clear genetic background and a number of disease genes have been identified. Mutations in the tau gene (MAPT) lead to frontotemporal dementia (FTD), whereas mutations in the genes for the amyloid-β precursor protein (APP) and the presenilins (PSEN1, PSEN2)...

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Detalles Bibliográficos
Autores principales: Pagnon de la Vega, María, Näslund, Carl, Brundin, RoseMarie, Lannfelt, Lars, Löwenmark, Malin, Kilander, Lena, Ingelsson, Martin, Giedraitis, Vilmantas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817590/
https://www.ncbi.nlm.nih.gov/pubmed/35120450
http://dx.doi.org/10.1186/s12864-022-08343-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817590/
https://www.ncbi.nlm.nih.gov/pubmed/35120450
http://dx.doi.org/10.1186/s12864-022-08343-9

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