CHMP2B mutations are not a common cause of frontotemporal lobar degeneration
- 1 May 2006
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 398 (1-2) , 83-84
- https://doi.org/10.1016/j.neulet.2005.12.056
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementiaNature Genetics, 2005
- The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementiaAnnals of Neurology, 2003
- Chromosome 3 linked frontotemporal dementia (FTD-3)Neurology, 2002
- Frontotemporal lobar degenerationNeurology, 1998
- AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseNature Genetics, 1998
- Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23Science, 1996
- Familial non-specific dementia maps to chromosome 3Human Molecular Genetics, 1995