Cite

    Daoud, H., Zhang, D., McMurray, F., Yu, A., Luco, S. M., Vanstone, J., Jarinova, O., Carson, N., Wickens, J., Shishodia, S., Choi, H., McDonough, M. A., Schofield, C. J., Harper, M., Dyment, D. A., & Armour, C. M. (2016). identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay. Journal of medical genetics, 53(3), 200–207. http://access.bl.uk/ark:/81055/vdc_100137791685.0x000042