Cite

    Jullien, L., Kannengiesser, C., Kermasson, L., Cormier‐Daire, V., Leblanc, T., Soulier, J., Londono‐Vallejo, A., de Villartay, J., Callebaut, I., & Revy, P. (2016). mutations of the RTEL1 Helicase in a Hoyeraal‐Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain. Human mutation, 37(5), 469–472. http://access.bl.uk/ark:/81055/vdc_100031855880.0x00001a