| 000 | 01743 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250518083418.0 | ||
| 264 | 0 | _c20210519 | |
| 008 | 202105s 0 0 eng d | ||
| 022 | _a1879-0542 | ||
| 024 | 7 |
_a10.1016/j.imlet.2020.01.008 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKhabbazi, Alireza | |
| 245 | 0 | 0 |
_aA new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran. _h[electronic resource] |
| 260 |
_bImmunology letters _c05 2020 |
||
| 300 |
_a27-32 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 |
_aAntibody Formation _xgenetics |
| 650 | 0 | 4 |
_aAutoimmunity _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aComputational Biology _xmethods |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 |
_aHereditary Autoinflammatory Diseases _xdiagnosis |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIran |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPhospholipase C gamma _xgenetics |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 | _aExome Sequencing |
| 700 | 1 | _aRahbar Kafshboran, Haniyeh | |
| 700 | 1 | _aNasiri Aghdam, Maryam | |
| 700 | 1 | _aNouri Nojadeh, Jafar | |
| 700 | 1 | _aDaghagh, Hossein | |
| 700 | 1 | _aDaneshmandpour, Yousef | |
| 700 | 1 | _aKazemzadeh, Mina | |
| 700 | 1 | _aHamzeiy, Hamid | |
| 700 | 1 | _aSakhinia, Ebrahim | |
| 773 | 0 |
_tImmunology letters _gvol. 221 _gp. 27-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.imlet.2020.01.008 _zAvailable from publisher's website |
| 999 |
_c30592331 _d30592331 |
||