Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17
- 1 November 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (5) , 1131-1138
- https://doi.org/10.1086/301594
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Genetic evidence for the involvement of τ in progressive supranuclear palsyAnnals of Neurology, 1997
- Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch familiesAnnals of Neurology, 1997
- The neuropathology of chromosome 17‐linked dementiaAnnals of Neurology, 1996
- Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21Human Molecular Genetics, 1996
- The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritanceNature Genetics, 1995
- Gerstmann‐Sträussler‐Scheinker Disease and the Indiana KindredBrain Pathology, 1995
- A Radiation Hybrid Map of the BRCA1 Region of Chromosome 17q12-q21Genomics, 1993
- Structure and novel exons of the human .tau. geneBiochemistry, 1992
- Rapidly progressive autosomal dominant parkinsonism and dementia with pallido‐ponto‐nigral degenerationAnnals of Neurology, 1992
- HEREDITARY PICK'S DISEASEBrain, 1982