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)

First Author: Ferguson A

Attributed to: Developing methods for identifying clinical phenotypes from routinely collected health data with applications to stroke genetics. funded by MRC

Abstract

No abstract provided

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