Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population

BACKGROUND: Type 1 diabetes is a multifactorial disease with a strong genetic component. The aim of the study was to assess the impact of single nucleotide polymorphisms (SNPs) in several genes as susceptible markers in the risk of type 1 diabetes in the Estonian population. Methods: The rs6679677 (...

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Detalles Bibliográficos
Autores principales: Douroudis, Konstantinos, Kisand, Kalle, Nemvalts, Virge, Rajasalu, Tarvo, Uibo, Raivo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830196/
https://www.ncbi.nlm.nih.gov/pubmed/20089178
http://dx.doi.org/10.1186/1471-2350-11-11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830196/
https://www.ncbi.nlm.nih.gov/pubmed/20089178
http://dx.doi.org/10.1186/1471-2350-11-11

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