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...

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Detalles Bibliográficos
Autores principales: Lee, Sanghoon, Kim, Bo Ram, Kim, Young Ok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Original Manuscript
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481157/
https://www.ncbi.nlm.nih.gov/pubmed/36217831
http://dx.doi.org/10.1177/00368504221131233

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