000 01494 a2200433 4500
005 20250518094006.0
264 0 _c20201201
008 202012s 0 0 eng d
022 _a1735-5249
024 7 _a10.18502/ijaai.v19i1.2422
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTalebi, Taravat
245 0 0 _aA Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency.
_h[electronic resource]
260 _bIranian journal of allergy, asthma, and immunology
_cFeb 2020
300 _a94-101 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdenosine Deaminase
_xdeficiency
650 0 4 _aAgammaglobulinemia
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIran
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aSevere Combined Immunodeficiency
_xgenetics
650 0 4 _aExome Sequencing
700 1 _aBiglari, Alireza
700 1 _aShahroeei, Mohammad
700 1 _aChangi-Ashtiani, Majid
700 1 _aDinmohammadi, Hossein
700 1 _aNavabi, Shadi Sadat
700 1 _aParvaneh, Nima
700 1 _aBossuyt, Xavier
700 1 _aShahani, Tina
700 1 _aRokni-Zadeh, Hassan
773 0 _tIranian journal of allergy, asthma, and immunology
_gvol. 19
_gno. 1
_gp. 94-101
856 4 0 _uhttps://doi.org/10.18502/ijaai.v19i1.2422
_zAvailable from publisher's website
999 _c30812904
_d30812904