Rare Sequence Variation Underlying Suspected Familial Cerebral Small‐Vessel Disease

Background Cerebral small‐vessel disease (cSVD) is the leading monogenic cause of stroke. Despite genetic screening in routine diagnosis, many cases remain without a known causative variant. Using a cohort with suspected familial cSVD and whole‐genome sequencing, we screened for variants in genes as...

Full description

Saved in:
Bibliographic Details
Main Authors: Bernard P. H. Cho, Kate Auckland, Stefan Gräf, Hugh S. Markus
Format: Article
Language:English
Published: Wiley 2024-08-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.123.035771
Tags: Add Tag
No Tags, Be the first to tag this record!