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In vivo staging of frontotemporal lobar degeneration TDP-43 type C pathology
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2 |
A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders
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3 |
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia
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4 |
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia
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BASE
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