Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family
- 1 February 2004
- journal article
- Published by Springer Science and Business Media LLC in neurogenetics
- Vol. 5 (1), 79-80
- https://doi.org/10.1007/s10048-003-0162-z
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM intervalMolecular Psychiatry, 2002
- Identification of a novel family of presenilin homologuesHuman Molecular Genetics, 2002
- Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.Brain, 2001
- Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear PalsyHuman Molecular Genetics, 1999
- Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22Neurology, 1998
- Presenilin mutations in Alzheimer's diseaseHuman Mutation, 1998
- A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.1994