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Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer’s Disease

✍ Scribed by El Kadmiri, N. (author);Zaid, N. (author);Zaid, Y. (author);Tadevosyan, A. (author);Hachem, A. (author);Dubé, M. P. (author);Hamzi, K. (author);El Moutawakil, B. (author);Slassi, I. (author);Nadifi, S. (author)

Book ID
121687505
Publisher
Elsevier Ltd
Year
2014
Tongue
English
Weight
656 KB
Volume
269
Category
Article
ISSN
0306-4522

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✍ Jill S. Goldman; Bruce Reed; Rosalie Gearhart; Joel H. Kramer; Bruce L. Miller 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 47 KB 👁 1 views

## Background: Early-onset familial alzheimer's disease (eofad) is linked to mutations in three autosomal dominant genes: ps1, ps2 and app. the clinical presentation and age of onset of mutations is variable. ## Objectives: The aim of this report is to describe a novel ps1 mutation believed to be