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A pathogenic PSEN2 p.His169Asn mutation associated with early-onset Alzheimer’s disease

BACKGROUND: Autosomal dominant early-onset Alzheimer’s disease (EOAD) is genetically heterogeneous and has been associated with mutations in 3 different genes, coding for amyloid precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2). Most frequent cases are associated with mutation...

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Bibliografische gegevens
Gepubliceerd in:Clin Interv Aging
Hoofdauteurs: Giau, Vo Van, Pyun, Jung-Min, Bagyinszky, Eva, An, Seong Soo A, Kim, SangYun
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Dove Medical Press 2018
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6074827/
https://ncbi.nlm.nih.gov/pubmed/30104866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CIA.S170374
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