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HLA-DRB1 gene polymorphisms in Iranian children with Henoch-Schönlein purpura
BACKGROUND: People 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 (HLAs). Among HLA genes, because of the high rate of polym...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996570/ https://www.ncbi.nlm.nih.gov/pubmed/29937904 http://dx.doi.org/10.4103/jrms.JRMS_344_17 |