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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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Main Authors: Weggen, Sascha, Beher, Dirk
格式: Artigo
語言:Inglês
出版: BioMed Central 2012
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3334542/
https://ncbi.nlm.nih.gov/pubmed/22494386
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/alzrt107
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