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EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder
J Lévy1,2,3, D Haye1, N Marziliano4
1Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
Haploinsufficiency of the EFNB2 gene, a regulator of nervous system development, is linked to developmental delays, congenital heart defects, and seizures in patients with 13qter deletions.
Area of Science:
- Genetics
- Developmental Biology
- Neurology
Background:
- Ephrin B2 (EFNB2) is a ligand for EphB receptors, crucial for nervous system development, neuronal migration, erythropoiesis, and vasculogenesis.
- Genetic variations in EFNB2 can impact these developmental processes.
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