Associated Papers
De Novo CUL3 Variant in a Child Presenting With Hypertension and Kidney Failure.
Peremans L et al.
Kidney International Reports, 2025
40677353 (PubMed )
Supplement: mmc1.pdf
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.
Laurie S et al.
Nature Medicine, 2025
39825153 (PubMed )
Supplement: 41591_2024_3420_MOESM3_ESM.xlsx › SuppTableS4.Disease_Causing
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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