Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
<p>Copy number variants (CNV) are established risk factors for neurodevelopmental disorders with seizures or epilepsy. With the hypothesis that seizure disorders share genetic risk factors, we pooled CNV data from 10,590 individuals with seizure disorders, 16,109 individuals with clinically va...
| Những tác giả chính: | , , , , , , , , , , , , , |
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| Tác giả khác: | |
| Định dạng: | Journal article |
| Ngôn ngữ: | English |
| Được phát hành: |
Springer Nature
2023
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