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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Alzheimers Dis |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2013
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| Θέματα: | |
| Διαθέσιμο Online: | 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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