An ABCC8 nonsense mutation causing neonatal diabetes through altered transcript expression di Flanagan, SE, Dũng, VC, Houghton, JAL, De Franco, E, Ngoc, CTB, Damhuis, A, Ashcroft, FM, Harries, LW, Ellard, S

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants di Johnston, JJ, van der Smagt, JJ, Rosenfeld, JA, Pagnamenta, AT, Alswaid, A, Baker, EH, Blair, E, Borck, G, Brinkmann, J, Craigen, W, Dung, VC, Emrick, L, Everman, DB, van Gassen, KL, Gulsuner, S, Harr, MH, Jain, M, Kuechler, A, Leppig, KA, McDonald-McGinn, DM, Can, NTB, Peleg, A, Roeder, ER, Rogers, RC, Sagi-Dain, L, Sapp, JC, Schäffer, AA, Schanze, D, Stewart, H, Taylor, JC, Verbeek, NE, Walkiewicz, MA, Zackai, EH, Zweier, C, Zenker, M, Lee, B, Biesecker, LG