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Familial emberger syndrome with autoimmunity, hyper-immunoglobulin E and lymphatic impairment caused by a novel GATA2 mutation

Autor: AlGassim, Moneerah, Al Seraihi, Ahad F., AlShaibani, AlFadel, Conca, Walter, AlShehri, Saleem, Moustafa Abouzied, Moheieldin, Hamadah, Issam, AlReshoodi, Saleh, Dasouki, Majed, Sheikh, Farrukh

Publikováno v: In Hematology/Oncology and Stem Cell Therapy May 2020

Familial Emberger Syndrome With Autoimmunity, Hyper-Immunoglobulin E and Lymphatic Impairment Caused by a Novel GATA2 Mutation.

Autor: AlGassim M; Department of Medicine, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Al Seraihi AF; Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK., AlShaibani A; Department of Hematology/Oncology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Conca W; Department of Medicine, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., AlShehri S; Department of Medicine, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Abouzied MM; Department of Radiology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Hamadah I; Department of Dermatology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., AlReshoodi S; Department of Radiology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Dasouki M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Sheikh F; Department of Medicine, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.

Publikováno v: Hematology/oncology and stem cell therapy [Hematol Oncol Stem Cell Ther] 2022 Jun 01; Vol. 15 (2), pp. 63-65. Date of Electronic Publication: 2022 Jun 01.