A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset
- 28 November 2000
- journal article
- case report
- Published by Wolters Kluwer Health in Neurology
- Vol. 55 (10) , 1590-1591
- https://doi.org/10.1212/wnl.55.10.1590
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation SpectrumAmerican Journal of Human Genetics, 1999
- Presenilins Interact with Armadillo Proteins Including Neural‐Specific Plakophilin‐Related Protein and β‐CateninJournal of Neurochemistry, 1999
- Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseHuman Molecular Genetics, 1995
- Misserise mutation of S182 gene in Italian families with early-onset Alzheimer's diseaseThe Lancet, 1995
- Italian multicentre study on dementia (SMID): A neuropsychological test battery for assessing Alzheimer's diseaseJournal of Psychiatric Research, 1990