| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3076507 | Neurología | 2010 | 4 Pages |
Abstract
E120G is a novel mutation in PSEN1 that probably causes early-onset autosomal dominant AD. Absence of genetic alterations in screening techniques (SSCP) does not rule out the presence of mutations. We recommend direct sequencing for the genetic study of patients with early-onset autosomal dominant AD.
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Authors
A. Lladó, R. Sánchez-Valle, M.J. Rey, P. Mercadal, C. Almenar, D. López-Villegas, J. Fortea, J.L. Molinuevo,