RAC3

Publications

Costain G et al. De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome. Genet Med.2019;21(4):1021–1026.  PMID: 30293988.

White JJ et al. WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. Am J Hum Genet. 2018;102(1):27–43.  PMID: 29276006.

Hiraide T et al. A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly. J Hum Genet. 2019;64(11):1127–1132.  PMID: 31420595.