000 01606 a2200469 4500
005 20250517200744.0
264 0 _c20191114
008 201911s 0 0 eng d
022 _a2213-2201
024 7 _a10.1016/j.jaip.2018.01.017
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHarris, Stephanie
245 0 0 _aMale X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease.
_h[electronic resource]
260 _bThe journal of allergy and clinical immunology. In practice
_c
300 _a1775-1777.e1 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aCells, Cultured
650 0 4 _aFemale
650 0 4 _aGenes, X-Linked
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aGranulomatous Disease, Chronic
_xdiagnosis
650 0 4 _aHematopoiesis
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHigh-Throughput Nucleotide Sequencing
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMosaicism
650 0 4 _aMutation
_xgenetics
650 0 4 _aNADPH Oxidase 2
_xgenetics
650 0 4 _aNeutrophil Activation
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
700 1 _aBraggins, Helen
700 1 _avan Leeuwen, Karin
700 1 _aGilmour, Kimberly
700 1 _aBuckland, Matthew S
700 1 _aRoos, Dirk
700 1 _aLowe, David M
773 0 _tThe journal of allergy and clinical immunology. In practice
_gvol. 6
_gno. 5
_gp. 1775-1777.e1
856 4 0 _uhttps://doi.org/10.1016/j.jaip.2018.01.017
_zAvailable from publisher's website
999 _c28053479
_d28053479