Human MD2 deficiency – an inborn error of immunity with pleiotropic features by Li, Y, Yu, Z, Schenk, M, Lagovsky, I, Illig, D, Walz, C, Rohlfs, M, Conca, R, Muise, AM, Snapper, SB, Uhlig, HH, Zion Garty, B, Klein, C, Kotlarz, D

Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy by Kotlarz, D, Marquardt, B, Barøy, T, Lee, W, Konnikova, L, Hollizeck, S, Magg, T, Lehle, A, Walz, C, Borggraefe, I, Hauck, F, Bufler, P, Conca, R, Wall, S, Schumacher, E, Misceo, D, Frengen, E, Bentsen, B, Uhlig, H, Hopfner, K, Muise, A, Snapper, S, Strømme, P, Klein, C

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease by Avitzur, Y, Avitzur, Y, Avitzur, Y, Guo, C, Mastropaolo, L, Bahrami, E, Chen, H, Zhao, Z, Elkadri, A, Elkadri, A, Elkadri, A, Dhillon, S, Murchie, R, Fattouh, R, Huynh, H, Walker, J, Wales, P, Cutz, E, Kakuta, Y, Dudley, J, Kammermeier, J, Powrie, F, Shah, N, Walz, C, Nathrath, M

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease. by Avitzur, Y, Guo, C, Mastropaolo, L, Bahrami, E, Chen, H, Zhao, Z, Elkadri, A, Dhillon, S, Murchie, R, Fattouh, R, Huynh, H, Walker, J, Wales, P, Cutz, E, Kakuta, Y, Dudley, J, Kammermeier, J, Powrie, F, Shah, N, Walz, C, Nathrath, M, Kotlarz, D, Puchaka, J, Krieger, JR, Racek, T