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APA Citation
Powis, Z., Petrik, I., Cohen, J., Escolar, D., Burton, J., van Ravenswaaij‐Arts, C., Sival, D., Stegmann, A., Kleefstra, T., Pfundt, R., Chikarmane, R., Begtrup, A., Huether, R., Tang, S., & Shinde, D. (2018). de novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. Clinical genetics, 93(5), 1030–1038. http://access.bl.uk/ark:/81055/vdc_100060303513.0x00005b