No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population
✍ Scribed by Afef Achouri Rassas, Sondess Hadj Fredj…
- Book ID
- 120919143
- Publisher
- Springer
- Year
- 2013
- Tongue
- English
- Weight
- 166 KB
- Volume
- 120
- Category
- Article
- ISSN
- 1435-1463
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## Wragg et al. [1996: Lancet 347:509-512] recorded an association between the intronbased presenilin 1 (PS1) genotype 1/1 and late-onset Alzheimer's disease (AD). This study was performed to determine if there is a similar association in the Chinese population. Ninety-one AD cases, 50 multiinfarc
Mutations in the Presenilin 1 (PS1) gene on chromosome 14 cause most early-onset familial Alzheimer's disease (AD). An intronic polymorphism in the PS1 gene was recently identified and reported to be associated with late-onset AD [Wragg et al., Lancet 347: 509-512, 1996]. The authors found an excess