A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. Al-Sulaiman R, Othman A, El-Akouri K, Fareed S, AlMulla H,...
Immune Dysregulation in Monogenic Inborn Errors of Immunity in Oman: Over A Decade of Experience From a Single Tertiary Center. Al Farsi T,...
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry. Jamee M, Azizi G, Baris S, Karakoc-Aydiner...