Farivar S

ORCID: 0000-0002-3277-1163 · 1 paper in corpus

2018

HLA-DRB1 gene polymorphisms in Iranian children with Henoch-Schönlein purpura.

Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences ·doi:10.4103/jrms.jrms_344_17

BackgroundPeople of all ages can suffer from Henoch-Schönlein purpura (HSP), but it is the most common vasculitis in childhood. The most important involving gene is located on chromosome 6p21.3, a region coding for human leukocyte antigens …