Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
Khan TN, Khan K, Sadeghpour A, Reynolds H, Perilla Y, McDonald MT, Gallentine WB, Baig SM, Task Force for Neonatal Genomics, Davis EE, et al. Am J Hum Genet. 2019 Jan 3; 104(1):94-111.