Publications

Hiatt SM, Neu MB, et al. De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay. PLoS Genet. 2018 Nov 30;14(11):e1007671. doi: 10.1371/journal.pgen.1007671. eCollection 2018 Nov. PMID: 30500825

Shieh JTC. Emerging RAS superfamily conditions involving GTPase function. PLoS Genet. 2019 Feb 14;15(2):e1007870. doi: 10.1371/journal.pgen.1007870. eCollection 2019 Feb. PMID: 30763311

Okamoto N, et al. RALA mutation in a patient with autism spectrum disorder and Noonan syndrome-like phenotype. N.Congenit Anom (Kyoto). 2019 Nov;59(6):195-196. doi: 10.1111/cga.12327. Epub 2019 Mar 8. PMID: 30761613