Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease
Main Authors: | , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMJ Publishing Group
2022-06-01
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Series: | Stroke and Vascular Neurology |
Online Access: | https://svn.bmj.com/content/7/3/182.full |