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The common rs13266634 C > T variant in SLC30A8 contributes to the heterogeneity of phenotype and clinical features of both type 1 and type 2 diabetic subtypes.
Acta Diabetol. 2022 Apr;59(4):545-552. doi: 10.1007/s00592-021-01831-6. Epub 2022 Jan 16.
Acta Diabetol. 2022.
PMID: 35034185
The associations between three genome-wide risk variants for serum C-peptide of T1D and autoantibody-positive T1D risk, and clinical characteristics in Chinese population.
Feng Y, Zhang Y, Chen Y, Chen S, Shen M, Fu Q, He Y, Liu Y, Hsu HT, Xu X, Chen H, Yang T, Xu K.
Feng Y, et al.
J Hum Genet. 2020 Mar;65(3):297-303. doi: 10.1038/s10038-019-0705-2. Epub 2019 Dec 12.
J Hum Genet. 2020.
PMID: 31827251
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