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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 en: | Indian J Endocrinol Metab |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acceso en liña: | 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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