Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency

Autor: Aydin, S.E., Freeman, A.F., Al-Herz, W., Al-Mousa, H.A., Arnaout, R.K., Aydin, R.C., Barlogis, V., Belohradsky, B.H., Bonfim, C., Bredius, R.G., Chu, J.I., Ciocarlie, O.C., Dogu, F., Gaspar, H.B., Geha, R.S., Gennery, A.R., Hauck, F., Hawwari, A., Hickstein, D.D., Hoenig, M., Ikinciogullari, A., Klein, C., Kumar, A., Ifversen, M.R.S., Matthes, S., Metin, A., Neven, B., Pai, S.Y., Parikh, S.H., Picard, C., Renner, E.D., Sanal, O., Schulz, A.S., Schuster, F., Shah, N.N., Shereck, E.B., Slatter, M.A., Su, H.C., Montfrans, J. van, Woessmann, W., Ziegler, J.B., Albert, M.H., Inborn Errors Working Party Europe, European Soc Primary Immunodefici

Publikováno v: Journal of Allergy and Clinical Immunology: In Practice, 7(3), 848-855. ELSEVIER SCIENCE BV
Journal of Allergy and Clinical Immunology: In Practice, 7(3), 848. Elsevier

BACKGROUND: Biallelic variations in the dedicator of cytokinesis 8 (DOCK8) gene cause a combined immunodeficiency with eczema, recurrent bacterial and viral infections, and malignancy. Natural disease outcome is dismal, but allogeneic hematopoietic s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94e9dd29744802a49599fac24a4b64f9
http://hdl.handle.net/1887/122185