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Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD
Cited 11 time in
Web of Science
Cited 11 time in Scopus
- Authors
- Issue Date
- 2010-05
- Publisher
- ELSEVIER SCI LTD
- Citation
- PARKINSONISM & RELATED DISORDERS; Vol.16(4); 305-306
- Abstract
- 1. Introduction
Mutations in the microtubule-associated protein tau gene
(MAPT) and progranulin gene (PGRN) have been identified in several
neurodegenerative disorders within the confines of the frontotemporal
lobar degeneration complex, including progressive supranuclear
palsy (PSP) and corticobasal syndrome (CBS) [1]. Although
most mutations in MAPT and PGRN have been indentified in familial
cases, mutations have also been described in sporadic cases.
In this study, we screened MAPT and PGRN mutation in a series
of Korean patients with sporadic PSP, CBS, and frontotemporal
dementia (FTD).
- ISSN
- 1353-8020
- Language
- English
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