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.

Clinical Genetics
|March 7, 2018
PubMed
Summary

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.

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