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- W2065254146 abstract "Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are considered to be part of a disease spectrum. However, with the exception of C9orf72, genes that cause ALS are rarely found to cause FTD and vice versa. To investigate this further, we have sequenced the ALS gene UBQLN2 in our FTD cohort and have found a single putative mutation. This further supports the concept that ALS genes are a rare cause of FTD." @default.
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- W2065254146 date "2015-01-01" @default.
- W2065254146 modified "2023-10-14" @default.
- W2065254146 title "A UBQLN2 variant of unknown significance in frontotemporal lobar degeneration" @default.
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- W2065254146 doi "https://doi.org/10.1016/j.neurobiolaging.2014.08.002" @default.
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