Associated Papers
Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants.
Priolo M et al.
European Journal of Human Genetics : Ejhg, 2023
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
Scala M et al.
Brain : a Journal of Neurology, 2022
De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome.
Costain G et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
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