Frontotemporal lobar degeneration in Finland:molecular genetics and clinical aspects

Frontotemporal lobar degeneration in Finland:molecular genetics and clinical aspects

Abstract Frontotemporal lobar degeneration (FTLD) is the second most common neurodegenerative disease leading to early-onset dementia (< 65 years), next to Alzheimer’s disease. FTLD is substantially a genetic disorder with up to 50% of cases having a positive family history. Mutati...

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Bibliographic Details
Main Author: Kaivorinne, A.-L. (Anna-Lotta)
Other Authors: Remes, A. (Anne)
Format: Doctoral Thesis
Language:English
Published: Oulun yliopisto 2012
Subjects:
C9ORF72
TAR DNA binding protein
charged multi-vesicular body protein 2B
dementia
frontotemporal dementia
frontotemporal lobar degeneration
genetics
haplotype
microtubule-associated protein tau
molecular genetics
mutation
phenotype
polymorphism
repeat expansion
geenit
geneettinen assosiaatioanalyysi
genetiikka
genotyyppi
molekyyligenetiikka
mutaatiot
otsa-ohimolohkorappeumat
Online Access:http://urn.fi/urn:isbn:9789526200132
http://nbn-resolving.de/urn:isbn:9789526200132

Internet

http://urn.fi/urn:isbn:9789526200132
http://nbn-resolving.de/urn:isbn:9789526200132

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