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...

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Bibliografiske detaljer
Udgivet i:J Med Genet
Main Authors: Zeldenrust, S R, Murrell, J, Farlow, M, Ghetti, B, Roses, A D, Benson, M D
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Publishing Group 1993
Fag:
Research Article
Online adgang: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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