Associated Papers
Complete loss of SLC30A8 in humans improves glucose metabolism and beta cell function.
Lamarche LB et al.
Diabetologia, 2025
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
32682410 (PubMed )
Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL2
Protective alleles and modifier variants in human health and disease.
Harper AR et al.
Nature Reviews. Genetics, 2015
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
Flannick J et al.
Nature Genetics, 2014
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