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TRA2B Gene Splice Variant Linked to Seizures and Neurodevelopmental Delay: A Second Case Study
Olga Shatokhina1, Valeriia Kovalskaia1, Peter Sparber1
1Federal State Budgetary Institution "Research Centre For Medical Genetics", 115478 Moscow, Russia.
Researchers identified a new TRA2B gene splice variant in a patient with seizures and neurodevelopmental delay. This finding reinforces previous research on TRA2B-related syndrome and its genetic causes.
Area of Science:
- Genetics
- Neurodevelopmental Disorders
- Molecular Biology
Background:
- The TRA2B gene plays a crucial role in RNA splicing.
- Pathogenic variants in TRA2B have been linked to neurodevelopmental disorders.
- Previous studies have identified TRA2B mutations, but further investigation is needed.
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