A Patient with Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene

Posterior cortical atrophy is a dementia syndrome with symptoms of cortical visual dysfunction, associated with amyloid plaques and neurofibrillary tangles predominantly affecting visual association cortex. Most patients diagnosed with posterior cortical atrophy will finally develop a typical Alzhei...

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Main Authors: Sitek, Emilia J., Narożańska, Ewa, Pepłońska, Beata, Filipek, Sławomir, Barczak, Anna, Styczyńska, Maria, Mlynarczyk, Krzysztof, Brockhuis, Bogna, Portelius, Erik, Religa, Dorota, Barcikowska, Maria, Sławek, Jarosław, Żekanowski, Cezary
格式: Artigo
語言:Inglês
出版: Public Library of Science 2013
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3625161/
https://ncbi.nlm.nih.gov/pubmed/23593396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0061074
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