Tau gene mutation in familial progressive subcortical gliosis
- 1 April 1999
- journal article
- research article
- Published by Springer Nature in Nature Medicine
- Vol. 5 (4), 454-457
- https://doi.org/10.1038/7454
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17Science, 1998
- Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of TauThe American Journal of Pathology, 1998
- Tau is a candidate gene for chromosome 17 frontotemporal dementiaAnnals of Neurology, 1998
- Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conferenceAnnals of Neurology, 1997
- Familial progressive subcortical gliosisNeurology, 1995
- Familial progressive subcortical gliosisNeurology, 1994
- Structure and novel exons of the human .tau. geneBiochemistry, 1992
- Tau proteins of alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoformsNeuron, 1992
- Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's diseaseNeuron, 1989
- PROGRESSIVE SUBCORTICAL GLIOSIS, A RARE FORM OF PRESENILE DEMENTIABrain, 1967