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Jump from pre-mutation to pathologic expansion in C9orf72
Zhengrui Xi1, Marka van Blitterswijk2, Ming Zhang1
1Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Street, Toronto, ON M5T 2S8, Canada.
American Journal of Human Genetics
|May 26, 2015
Summary
The C9orf72 G4C2 repeat expansion, a cause of ALS and FTLD, may have multiple origins. Small expansions (pre-mutations) can enlarge during transmission, leading to disease in subsequent generations.
Area of Science:
- Genetics
- Neurodegenerative Diseases
Background:
- The C9orf72 G4C2 repeat expansion is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD).
- The lower limit for pathological expansions remains undefined, with a suggested cutoff of 30 repeats.
- Previous hypotheses suggested a single origin for the expansion, followed by population-wide spread.
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