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De-coding genetic risk variants in type 1 diabetes
The conceptual basis for a genetic predisposition underlying the risk for developing type 1 diabetes (T1D) predates modern human molecular genetics. Over half of the genetic risk has been attributed to the human leukocyte antigen (HLA) class II gene region and to the insulin (INS) gene locus – both...
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| Pubblicato in: | Immunol Cell Biol |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8119379/ https://ncbi.nlm.nih.gov/pubmed/33483996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/imcb.12438 |
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