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Scientific Article
unige:114066 
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The CST3 B haplotype is associated with frontotemporal lobar degeneration |
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| Authors | ||
| Published in | European Journal of Neurology. 2010, vol. 17, no. 1, p. 143-146 | |
| Abstract | Frontotemporal lobar degeneration (FTLD) is a common cause of early-onset dementia. Given the role of cystatin C in brain neurodegeneration and neuroregeneration, the aim of this study was to determine whether the cystatin C gene (CST3) was genetically associated with FTLD. | |
| Keywords | Aged — Brain/metabolism/pathology/physiopathology — Cystatin C/genetics — DNA Mutational Analysis — Female — Frontotemporal Lobar Degeneration/genetics/metabolism/physiopathology — Genetic Markers/genetics — Genetic Predisposition to Disease/genetics — Genetic Testing — Haplotypes/genetics — Humans — Intercellular Signaling Peptides and Proteins/genetics — Male — Middle Aged — Progranulins — Risk Factors | |
| Identifiers | PMID: 19674067 | |
| Full text | ||
| Citation (ISO format) | BENUSSI, L et al. The CST3 B haplotype is associated with frontotemporal lobar degeneration. In: European Journal of Neurology, 2010, vol. 17, n° 1, p. 143-146. https://archive-ouverte.unige.ch/unige:114066 |
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