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Presenilin mutations and their impact on neuronal differentiation in Alzheimer’s disease
The presenilin genes (PSEN1 and PSEN2) are mainly responsible for causing early-onset familial Alzheimer’s disease, harboring ~300 causative mutations, and representing ~90% of all mutations associated with a very aggressive disease form. Presenilin 1 is the catalytic core of the γ-secretase complex...
Autores principales: | Hernández-Sapiéns, Mercedes A., Reza-Zaldívar, Edwin E., Márquez-Aguirre, Ana L., Gómez-Pinedo, Ulises, Matias-Guiu, Jorge, Cevallos, Ricardo R., Mateos-Díaz, Juan C., Sánchez-González, Víctor J., Canales-Aguirre, Alejandro A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451546/ https://www.ncbi.nlm.nih.gov/pubmed/34100423 http://dx.doi.org/10.4103/1673-5374.313016 |
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