Molecular consequences of amyloid precursor protein and presenilin mutations causing autosomal-dominant Alzheimer's disease

Mutations in both the amyloid precursor protein (APP) and the presenilin (PSEN) genes cause familial Alzheimer's disease (FAD) with autosomal dominant inheritance and early onset of disease. The clinical course and neuropathology of FAD and sporadic Alzheimer's disease are highly similar,...

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Detalles Bibliográficos
Autores principales: Weggen, Sascha, Beher, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334542/
https://www.ncbi.nlm.nih.gov/pubmed/22494386
http://dx.doi.org/10.1186/alzrt107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334542/
https://www.ncbi.nlm.nih.gov/pubmed/22494386
http://dx.doi.org/10.1186/alzrt107

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