论文信息 - Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis - 字舞流文

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

P. V. Van Caeseele | G. Cuvelier | C. Rockman‐Greenberg | M. Schroeder | Tamar S. Rubin | L. Kwan

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[3] P. V. Van Caeseele,et al. Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases , 2014, Molecular genetics and metabolism reports.

[4] S. Grazioli,et al. Limitation of TREC-based newborn screening for ZAP70 Severe Combined Immunodeficiency. , 2014, Clinical immunology.

[5] U. Pannicke,et al. Deficiency of innate and acquired immunity caused by an IKBKB mutation. , 2013, The New England journal of medicine.