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Rates of rare copy number variants in different circumstances among patients with genetic developmental and epileptic encephalopathy
BACKGROUND: Most patients with developmental and epileptic encephalopathy (DEE) have genetic etiology, which has been uncovered with different methods. Although chromosomal microarray analysis (CMA) has been broadly used in patients with DEE, data is still limited. METHODS: Among 560 children (<1...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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SAGE Publications
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481157/ https://www.ncbi.nlm.nih.gov/pubmed/36217831 http://dx.doi.org/10.1177/00368504221131233 |