학술논문

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Document Type
Article
Source
Nature Communications; 7/20/2023, Issue 1, p1-19, 19p
Subject
SEIZURES (Medicine)
DNA copy number variations
22Q11 deletion syndrome
GENETIC disorders
HUMAN phenotype
PHENOTYPES
SHORT tandem repeat analysis
EPILEPSY
Language
ISSN
20411723
Abstract
Copyright of Nature Communications is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)