Genetic Influences on Atrophy Patterns in Familial Alzheimer’s Disease: A Comparison of APP and PSEN1 Mutations

Mutations in the presenilin1 (PSEN1) and amyloid β-protein precursor (APP) genes account for the majority of cases of autosomal dominantly inherited Alzheimer’s disease (AD). We wished to assess and compare the patterns of cerebral loss produced by these two groups of mutations. Volumetric magnetic...

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Bibliografiset tiedot
Julkaisussa:J Alzheimers Dis
Päätekijät: Scahill, Rachael I., Ridgway, Gerard R., Bartlett, Jonathan W., Barnes, Josephine, Ryan, Natalie S., Mead, Simon, Beck, Jonathan, Clarkson, Matthew J., Crutch, Sebastian J., Schott, Jonathan M., Ourselin, Sebastien, Warren, Jason D., Hardy, John, Rossor, Martin N., Fox, Nick C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2013
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4982537/
https://ncbi.nlm.nih.gov/pubmed/23380992
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JAD-121255
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