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Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD

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Authors
Kim, Han-Joon; Jeon, Beom S.; Yun, Ji Young; Seong, Moon-Woo; Lee, Jee-Young; Park, Sung Sup
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
URI
https://hdl.handle.net/10371/77682
DOI
https://doi.org/10.1016/j.parkreldis.2010.01.004
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College of Medicine/School of Medicine (의과대학/대학원)Dept. of Neurology (신경과학교실)Journal Papers (저널논문_신경과학교실)
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