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APA Citation
Bina, R., Matalon, D., Fregeau, B., Tarsitano, J. J., Aukrust, I., Houge, G., Bend, R., Warren, H., Stevenson, R. E., Stuurman, K. E., Barkovich, A. J., & Sherr, E. H. (2020). de novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of medical genetics, 57(7), 461–465. http://access.bl.uk/ark:/81055/vdc_100137786806.0x00003b