Art
J-GLOBAL ID:201802237764462622   Reference number:18A0975344

Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer’s disease: analysis of Osaka mutation-knockin mice

APP機能の突然変異誘発性消失は劣性家族性Alzheimer病におけるGABA作動性枯渇を引き起こす: 大阪突然変異-ノックインマウスの分析【JST・京大機械翻訳】
Author (21):
Material:
Volume:Issue:Page: 59  Publication year: 2017 
JST Material Number: U7296A  ISSN: 2051-5960  Document type: Article
Article type: 原著論文  Country of issue: United Kingdom (GBR)  Language: ENGLISH (EN)
Abstract/Point:
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Japanese summary of the article(about several hundred characters).
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The E693Δ (Osaka) mutation in ...
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JST classification (5):
JST classification
Category name(code) classified by JST.
Nervous system diseases  ,  Basic neurology  ,  Genetic variation  ,  Cell physiology in general  ,  Biological function 
Substance index (1):
Substance index
Chemical Substance indexed to the Article.
Reference (32):

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