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No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden.
- Source :
-
Amyotrophic lateral sclerosis & frontotemporal degeneration [Amyotroph Lateral Scler Frontotemporal Degener] 2013 Jan; Vol. 14 (1), pp. 26-9. Date of Electronic Publication: 2012 Sep 17. - Publication Year :
- 2013
-
Abstract
- An intronic GGGGCC-hexanucleotide repeat expansion in C9ORF72 was recently identified as a major cause of amyotrophic lateral sclerosis and frontotemporal dementia. Some amyotrophic lateral sclerosis patients have signs of parkinsonism, and many parkinsonism patients develop dementia. In this study we examined if the hexanucleotide repeat expansion was present in parkinsonism patients, to clarify if there could be a relationship between the repeat expansion and disease. We studied the size of the hexanucleotide repeat expansion in a well defined population-based cohort of 135 Parkinson's disease patients and 39 patients with atypical parkinsonism and compared with 645 Swedish control subjects. We found no correlation between Parkinson's disease or atypical parkinsonism and the size of the GGGGCC repeat expansion in C9ORF72. In conclusion, this GGGGCC-repeat expansion in C9ORF72 is not a cause of parkinsonism in the Swedish population.
- Subjects :
- Aged
Base Sequence
C9orf72 Protein
Female
Genetic Markers genetics
Humans
Linkage Disequilibrium genetics
Male
Middle Aged
Molecular Sequence Data
Prevalence
Risk Factors
Sweden epidemiology
DNA Repeat Expansion genetics
Genetic Predisposition to Disease epidemiology
Genetic Predisposition to Disease genetics
Parkinson Disease epidemiology
Parkinson Disease genetics
Polymorphism, Single Nucleotide genetics
Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2167-9223
- Volume :
- 14
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Amyotrophic lateral sclerosis & frontotemporal degeneration
- Publication Type :
- Academic Journal
- Accession number :
- 22985429
- Full Text :
- https://doi.org/10.3109/17482968.2012.725415