Open AccessDominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
Author(s) -
V. Béziat,
S.J. Tavernier,
Y.-H. Chen,
C.S. Ma,
M. Materna,
A. Laurence,
J. Staal,
D. Aschenbrenner,
L. Roels,
L. Worley,
K. Claes,
L. Gartner,
L.A. Kohn,
M. de Bruyne,
K. Schmitz-Abe,
L.-M. Charbonnier,
S. Keles,
J. Nammour,
N. Vladikine,
M.R.L.M. Renkilaraj,
Yoann Seeleuthner,
M. Migaud,
J. Rosain,
M. Jeljeli,
B. Boisson,
Eva Van Braeckel,
J.A. Rosenfeld,
Ha Van Dai,
L.C. Burrage,
D.R. Murdock,
B.N. Lambrecht,
V. Avettand-Fenoel,
T.P. Vogel,
C.R. Esther,
S. Haskologlu,
F. Dogu,
P. Ciznar,
D. Boutboul,
M. Ouachée-Chardin,
J. Amourette,
M.-N. Lebras,
C. Gauvain,
C. Tcherakian,
A. Ikinciogullari,
R. Beyaert,
L. Abel,
J.D. Milner,
B. Grimbacher,
L.-J. Couderc,
M.J. Butte,
A.F. Freeman,
É. Catherinot,
C. Fieschi,
T.A. Chatila,
S.G. Tangye,
H.H. Uhlig,
F. Haerynck,
J.-L. Casanova,
A. Puel,
Undiagnosed Diseases Network
Publication year - 2020
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - Uncategorized
DOI - 10.17615/tv0q-me94
Subject(s) - immunoglobulin e , biology , genetics , immunology , antibody