Publications
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Author Title [ Year
] Filters: Author is Stray-Pedersen, Asbjørg and Keyword is Immunologic Deficiency Syndromes [Clear All Filters]
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia. Am J Hum Genet 95, 96-107 (2014).
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. J Allergy Clin Immunol 139, 232-245 (2017).
