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APA Citation
Brereton, E., Fassi, E., Araujo, G. C., Dodd, J., Telegrafi, A., Pathak, S. J., & Shinawi, M. (2018). mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities. Molecular genetics & genomic medicine, 6(2), 294–300. http://access.bl.uk/ark:/81055/vdc_100059836650.0x00000a