Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder.
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Blackburn PR, et al. Among authors: jech r.
medRxiv [Preprint]. 2023 Jun 16:2023.06.13.23290941. doi: 10.1101/2023.06.13.23290941.
medRxiv. 2023.
PMID: 37398376
Free PMC article.
Updated.
Preprint.