000 01414 a2200373 4500
005 20250517223250.0
264 0 _c20190723
008 201907s 0 0 eng d
022 _a1531-6963
024 7 _a10.1097/BOR.0000000000000532
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAeschlimann, Florence A
245 0 0 _aHaploinsufficiency of A20 and other paediatric inflammatory disorders with mucosal involvement.
_h[electronic resource]
260 _bCurrent opinion in rheumatology
_c09 2018
300 _a506-513 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aBehcet Syndrome
_xgenetics
650 0 4 _aChild
650 0 4 _aFamilial Mediterranean Fever
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHaploinsufficiency
_xgenetics
650 0 4 _aHereditary Autoinflammatory Diseases
_xgenetics
650 0 4 _aHumans
650 0 4 _aLymphadenitis
_xgenetics
650 0 4 _aMevalonate Kinase Deficiency
_xgenetics
650 0 4 _aMutation
650 0 4 _aPharyngitis
_xgenetics
650 0 4 _aPyrin
_xgenetics
650 0 4 _aStomatitis, Aphthous
_xgenetics
650 0 4 _aTumor Necrosis Factor alpha-Induced Protein 3
_xgenetics
700 1 _aLaxer, Ronald M
773 0 _tCurrent opinion in rheumatology
_gvol. 30
_gno. 5
_gp. 506-513
856 4 0 _uhttps://doi.org/10.1097/BOR.0000000000000532
_zAvailable from publisher's website
999 _c28544231
_d28544231