Dominant LMAN2L mutation causes intellectual disability with remitting epilepsy

Reem A Alkhater1,2, Peixiang Wang1, Alessandra Ruggieri3

  • 1Program in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.

Summary

Mutations in LMAN2L cause epilepsy and intellectual disability by disrupting glycoprotein secretion. This study identifies a new autosomal dominant mutation leading to LMAN2L mislocalization and brain development issues.

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