Article ID Journal Published Year Pages File Type
6066370 Journal of Allergy and Clinical Immunology 2014 9 Pages PDF
Abstract
In patients with DOCK8 deficiency, only certain combinations of germline mutations supported secondary somatic repair. Those patients had an ameliorated disease course with longer survival but still had fatal complications or required hematopoietic cell transplantation. These observations support the concept that some DOCK8-immunodeficient patients have mutable mosaic genomes that can modulate disease phenotype over time.
Related Topics
Life Sciences Immunology and Microbiology Immunology
Authors
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