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APA Citation
Cohen, J., Srivastava, S., Farwell Hagman, K., Shinde, D., Huether, R., Darcy, D., Wallerstein, R., Houge, G., Berland, S., Monaghan, K., Poretti, A., Wilson, A., Chung, W., & Fatemi, A. (2017). further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features. Clinical genetics, 91(5), 697–707. http://access.bl.uk/ark:/81055/vdc_100045507457.0x000060