Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants
Abstract
The main genetic risk factors for progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) are located at chromosome 17q21.31. The identification of risk H1 subhaplotypes suggests that disease-specific variants can be identified by resequencing the 17q21.31 region (1.4 Mb) in carriers of risk H1 subhaplotypes. We hypothesized that PSP/CBD H1 subhaplotype carriers could have undergone a mutational event absent among unaffected...
Paper Details
Title
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants
Published Date
Jun 1, 2018
Journal
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