Cite

    Janecke, A. R., Xu, R., Steichen‐Gersdorf, E., Waldegger, S., Entenmann, A., Giner, T., Krainer, I., Huber, L. A., Hess, M. W., Frishberg, Y., Barash, H., Tzur, S., Schreyer‐Shafir, N., Sukenik–Halevy, R., Zehavi, T., Raas‐Rothschild, A., Mao, C., & Müller, T. (2017). deficiency of the sphingosine‐1‐phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications. Human mutation, 38(4), 365–372. http://access.bl.uk/ark:/81055/vdc_100044358433.0x000006