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TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls
Background: Celiac disease (CD) is a genetically complex autoimmune disease which is triggered by dietary gluten. Human leukocyte antigen (HLA) class II genes are known to act as high-risk markers for CD, where >95% of CD patients carry (HLA), DQ2 and/or DQ8 alleles. Therefore, the present study...
Guardat en:
| Publicat a: | Biosci Rep |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Portland Press Ltd.
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8202064/ https://ncbi.nlm.nih.gov/pubmed/34042155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20210509 |
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