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2. Comprehensive analysis of the mutation spectrum in 301 German ALS families

3. Hot-spot KIF5A mutations cause familial ALS

4. Sequence variations in C9orf72 downstream of the hexanucleotide repeat region and its effect on repeat-primed PCR interpretation: a large multinational screening study.

5. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts

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