000 | 01842 a2200529 4500 | ||
---|---|---|---|
005 | 20250518032804.0 | ||
264 | 0 | _c20200402 | |
008 | 202004s 0 0 eng d | ||
022 | _a1521-7035 | ||
024 | 7 |
_a10.1016/j.clim.2019.03.010 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aTuijnenburg, Paul | |
245 | 0 | 0 |
_aPathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency. _h[electronic resource] |
260 |
_bClinical immunology (Orlando, Fla.) _c06 2019 |
||
300 |
_a23-27 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAdrenal Insufficiency _xcongenital |
650 | 0 | 4 |
_aAnkyrin Repeat _xgenetics |
650 | 0 | 4 |
_aB-Lymphocytes _ximmunology |
650 | 0 | 4 | _aCells, Cultured |
650 | 0 | 4 |
_aCommon Variable Immunodeficiency _xgenetics |
650 | 0 | 4 | _aEctodermal Dysplasia |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aImmunoglobulin Class Switching _xgenetics |
650 | 0 | 4 | _aImmunologic Memory |
650 | 0 | 4 | _aImmunophenotyping |
650 | 0 | 4 | _aLymphocyte Activation |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 |
_aNF-kappa B p52 Subunit _xgenetics |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 |
_aReceptors, CXCR5 _xmetabolism |
650 | 0 | 4 |
_aT-Lymphocytes _ximmunology |
700 | 1 | _aLango Allen, Hana | |
700 | 1 | _ade Bree, Godelieve J | |
700 | 1 | _aSavic, Sinisa | |
700 | 1 | _aJansen, Machiel H | |
700 | 1 | _aStockdale, Claire | |
700 | 1 | _aSimeoni, Ilenia | |
700 | 1 | _aTen Berge, Ineke J M | |
700 | 1 | _avan Leeuwen, Ester M M | |
700 | 1 | _aThaventhiran, James E | |
700 | 1 | _aKuijpers, Taco W | |
773 | 0 |
_tClinical immunology (Orlando, Fla.) _gvol. 203 _gp. 23-27 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.clim.2019.03.010 _zAvailable from publisher's website |
999 |
_c29558143 _d29558143 |