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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...
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| Publicado no: | J Res Med Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5996570/ https://ncbi.nlm.nih.gov/pubmed/29937904 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jrms.JRMS_344_17 |
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