Cite

    Bursztejn, A., Briggs, T., del Toro Duany, Y., Anderson, B., O'Sullivan, J., Williams, S., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G., Hur, S., & Crow, Y. (n.d.). unusual cutaneous features associated with a heterozygous gain‐of‐function mutation in IFIH1: overlap between Aicardi‐Goutières and Singleton‐Merten syndromes. British journal of dermatology, 173, 1505–1513. http://access.bl.uk/ark:/81055/vdc_100172214490.0x000048