دورية أكاديمية

Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature

التفاصيل البيبلوغرافية
العنوان: Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature
المؤلفون: Fallahi, Mazdak, Jamee, MahnazAff2, IDs13223022007490_cor2, Enayat, Javad, Abdollahimajd, FahimehAff3, Aff4, Mesdaghi, Mehrnaz, Khoddami, Maliheh, Segarra-Roca, AnnaAff6, Aff7, Frohne, AlexandraAff6, Aff7, Dmytrus, JasminAff6, Aff7, Keramatipour, Mohammad, Mansouri, Mahboubeh, Eslamian, Golnaz, Fallah, Shahrzad, Boztug, KaanAff6, Aff8, Aff9, Aff10, Aff11, Chavoshzadeh, ZahraAff1, IDs13223022007490_cor15
المصدر: Allergy, Asthma & Clinical Immunology. 18(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:17101492
DOI:10.1186/s13223-022-00749-0