Login / Signup

A novel splice site CUL3 variant in a patient with neurodevelopmental delay.

Krista M VincentDanielle K Bourque
Published in: Brain & development (2023)
This is the first report of an individual with a splice site variant causing CUL3-related neurodevelopmental disorder and expands our understanding of this rare condition.
Keyphrases
  • case report
  • congenital heart disease