Associated Papers
Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.
Blackburn PR et al.
Annals of Neurology, 2024
Are CUL3 variants an underreported cause of congenital heart disease?
Di Francesco D et al.
American Journal of Medical Genetics. Part A, 2023
Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder.
Blackburn PR et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
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