Exome sequencing in Nigerian children with early‐onset epilepsy syndromes
Abstract Objective Nigeria, along with other Sub‐Saharan African countries, bears the highest burden of epilepsy worldwide. This high prevalence is attributed to a combination of factors, including a significant incidence of infectious diseases, perinatal complications, and genetic etiologies. Genet...
Saved in:
Main Authors: | Ibitayo Abigail Ademuwagun, Yagoub Adam, Solomon Oladapo Rotimi, Steffen Syrbe, Maximilian Radtke, Julia Hentschel, Johannes R. Lemke, Ezekiel Adebiyi |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2025-02-01
|
Series: | Epilepsia Open |
Subjects: | |
Online Access: | https://doi.org/10.1002/epi4.13106 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38
by: Mostafa Neissi, et al.
Published: (2025-02-01) -
Refining management strategies for Lennox–Gastaut syndrome: Updated algorithms and practical approaches
by: Stéphane Auvin, et al.
Published: (2025-02-01) -
Whole Exome Sequencing Reveals Rare Variants in Genes Associated with Metabolic Disorders in Women with PCOS
by: Priyal Sharma, et al.
Published: (2023-10-01) -
SNP discovery by exome capture and resequencing in a pea genetic resource collection
by: Aubert, Grégoire, et al.
Published: (2023-10-01) -
Successful management of refractory epilepsy in creatine transporter deficiency with cannabidiol and clobazam: A case report
by: Maria Borrell‐Pichot, et al.
Published: (2025-02-01)