Zobrazeno 1 - 1
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pro vyhledávání: '"Latifa Al Shekaili"'
Autor:
Sulaiman Al Gazlan, Bander Al Saud, Saleh Al Mohsen, Abbas Hawwari, Latifa Al Shekaili, Ammar AlKawi, Mufarreh Al Zahrani, Abdulaziz Al Ghonaium, Agha M. Rehan Khaliq, Farrukh Sheikh, Hasan Al Dhekri, Hamoud Al Mousa, Safiah Al Sumayli, Rand Arnaout, Anas Dababo
Publikováno v:
Clinical Immunology. 178:39-44
Background Hyper-IgE syndrome (HIES) due to DOCK8 deficiency is an autosomal recessive (AR) primary combined immunodeficiency which results in significant morbidity and mortality at a young age. Different mutations in the DOCK8 gene can lead to varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e2a90197f35c08ece6e0e7d9a0c115
https://doi.org/10.1016/j.clim.2016.08.002
https://doi.org/10.1016/j.clim.2016.08.002
