Frequency and phenotype associations of rare variants in five monogenic cerebral small vessel disease genes in 200,000 UK Biobank participants with whole exome sequencing data (2021)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2021.11.17.21266447
Publication URI: http://dx.doi.org/10.1101/2021.11.17.21266447
Type: Preprint