Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis

scientific article published on 04 October 2018

Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S10875-018-0555-2
P698PubMed publication ID30288645

P50authorCheryl Rockman-GreenbergQ40286334
Paul Van CaeseeleQ114718272
P2093author name stringMarlis L Schroeder
Geoffrey D E Cuvelier
Tamar S Rubin
Luvinia Kwan
P2860cites workRetrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseasesQ37434063
Immunodeficiency associated with a nonsense mutation of IKBKB.Q41741343
Deficiency of innate and acquired immunity caused by an IKBKB mutation.Q42247188
Limitation of TREC-based newborn screening for ZAP70 Severe Combined Immunodeficiency.Q53053269
P433issue7
P407language of work or nameEnglishQ1860
P304page(s)742-744
P577publication date2018-10-04
P1433published inJournal of Clinical ImmunologyQ6294961
P1476titleNewborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis
P478volume38

Reverse relations

Q58582861Clinical presentation, immunologic features, and hematopoietic stem cell transplant outcomes for IKBKB immune deficiencycites workP2860

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