Successful engraftment of donor marrow following allogeneic hematopoietic cell transplantation in autosomal recessive Hyper IgE syndrome due to DOCK8 deficiency

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.

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Detalhes bibliográficos
Main Authors: McDonald, Douglas R., Massaad, Michel J., Johnston, Alicia, Keles, Sevgi, Chatila, Talal, Geha, Raif S., Pai, Sung-Yun
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2998541/
https://ncbi.nlm.nih.gov/pubmed/20810158
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2010.07.034
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