Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants (2022)

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

No abstract provided

Type: Journal Article/Review

Parent Publication: Neurology Genetics

Issue: 5