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

Rubin, Tamar S

Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis. [electronic resource] - Journal of clinical immunology 10 2018 - 742-744 p. digital

Publication Type: Letter

1573-2592

10.1007/s10875-018-0555-2 doi


Alleles
DNA Mutational Analysis
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Humans
I-kappa B Kinase--deficiency
Infant, Newborn
Mutation
Neonatal Screening
Phenotype
Severe Combined Immunodeficiency--diagnosis