First patient in the Iranian Registry with novel DOCK2 gene mutation, presenting with skeletal tuberculosis, and review of literature

Autor: Sharifinejad, Niusha, Sadri, Homa, Kalantari, Arash, Delavari, Samaneh, Noohi, Amirhosein, Aminpour, Yasaman, Sabzevari, Araz, Azizi, Gholamreza

Publikováno v: Allergy, Asthma & Clinical Immunology, Vol 17, Iss 1, Pp 1-8 (2021)
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology

Background Dedicator of cytokinesis 2 (DOCK2) deficiency is an inborn error of immunity characterized by cellular and humoral immunological abnormalities leading to early-onset infections. Case presentation We reported a novel case of a 27 months old

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df2fce7a4415b7e9dd6e1ffb3f9ec1ea
https://doaj.org/article/7c352c1215f84e3a9a4aa26e4c8ccf6a

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.