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- W2774907112 abstract "Background: Over the past years, whole-exome sequencing (WES) has become a widespread diagnostic tool in a broad spectrum of heterogeneous neurological disorders with a suspected monogenetic (Mendelian) aetiology. To date, several studies have addressed the utility of next-generation sequencing methods, reporting diagnostic yields of approximately 25%." @default.
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- W2774907112 date "2017-10-01" @default.
- W2774907112 modified "2023-10-18" @default.
- W2774907112 title "Diagnostic yield of whole-exome sequencing in neurological diaseases" @default.
- W2774907112 doi "https://doi.org/10.1016/j.jns.2017.08.468" @default.
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