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PTPN22 1858 C/T Exon Polymorphism is not Associated with Graves' Disease in Kashmiri population
BACKGROUND: Graves' disease (GD) is a multifactorial autoimmune disease with contribution from both genetic and epigenetic factors in its causation. Association of genetic factors and GD has been extensively studied. Gene “protein tyrosine phosphatase nonreceptor 22” (PTPN22) is an important im...
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| Publicado no: | Indian J Endocrinol Metab |
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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/PMC6085953/ https://ncbi.nlm.nih.gov/pubmed/30148088 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijem.IJEM_105_18 |
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