Case Report: A 3’ splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child
The RORB (Retinoic Acid Receptor-related orphan receptor β) gene plays a crucial role in neurodevelopment and is strongly associated with bipolar disorder, cognitive function, and Alzheimer’s disease. Recently, RORB has also emerged as a novel potential gene involved in generalized epilepsy and abse...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-01-01
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| Series: | Frontiers in Genetics |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2024.1508922/full |
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