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RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

Familial Alzheimer's disease (FAD) has been shown to be associated with three distinct point mutations within the same codon of the amyloid precursor protein (APP) gene. The mutation identified in the Indiana kindred is a G-->T transversion at the first position of the codon for amino acid 7...

詳細記述

保存先:
書誌詳細
出版年:J Med Genet
主要な著者: Zeldenrust, S R, Murrell, J, Farlow, M, Ghetti, B, Roses, A D, Benson, M D
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Publishing Group 1993
主題:
オンライン・アクセス:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016419/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7686976/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.6.476
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