Elsevier, Journal of Allergy and Clinical Immunology, 6(126), p. 1304-1305.e3, 2010
DOI: 10.1016/j.jaci.2010.07.034
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A child with homozygous partial deletion of the DOCK8 gene showed characteristic clinical findings of autosomal recessive hyper-IgE syndrome and full donor chimerism early after matched sibling bone marrow transplantation.