| 000 | 01708 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250517122732.0 | ||
| 264 | 0 | _c20170130 | |
| 008 | 201701s 0 0 eng d | ||
| 022 | _a1578-1267 | ||
| 024 | 7 |
_a10.1016/j.aller.2016.08.005 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFazel, A | |
| 245 | 0 | 0 |
_aNovel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity. _h[electronic resource] |
| 260 |
_bAllergologia et immunopathologia _c |
||
| 300 |
_a82-86 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAdrenal Cortex Hormones _xtherapeutic use |
| 650 | 0 | 4 |
_aAutoimmunity _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aCytidine Deaminase _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDwarfism, Pituitary _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aGrowth Hormone _xtherapeutic use |
| 650 | 0 | 4 | _aHormone Replacement Therapy |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyper-IgM Immunodeficiency Syndrome _xgenetics |
| 650 | 0 | 4 |
_aImmunoglobulin M _xblood |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aIran |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aAICDA (Activation-Induced Cytidine Deaminase) |
| 700 | 1 | _aKashef, S | |
| 700 | 1 | _aAleyasin, S | |
| 700 | 1 | _aHarsini, S | |
| 700 | 1 | _aKaramizadeh, Z | |
| 700 | 1 | _aZoghi, S | |
| 700 | 1 | _aFlores, S K | |
| 700 | 1 | _aBoztug, K | |
| 700 | 1 | _aRezaei, N | |
| 773 | 0 |
_tAllergologia et immunopathologia _gvol. 45 _gno. 1 _gp. 82-86 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.aller.2016.08.005 _zAvailable from publisher's website |
| 999 |
_c26556432 _d26556432 |
||