Variants in the hepatocyte nuclear factor-1 alpha and-4alpha genes in Finnish and Chinese subjects with late-onset type 2 diabetes
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The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: Evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands
Urhammer SA, Hansen T, Ekstrom CT, et al. The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands [J]. Clin Endocrinol Metab, 1998, 83(12): 4506-4509.
A missense mutation in the glucagon receptor gene is associated with mon-insulin-dependent diabtes mellitus
Hager J, Hansen L, Vaisse C, et al. A missense mutation in the glucagon receptor gene is associated with mon-insulin-dependent diabtes mellitus[J]. Nature Genetics, 1995, 9: 299-304.
Mutation in mitochnodrial tRNA (Leu) (UUR) gene in a large pedigree with maternally transmitted type II DM and deafness
Vanden JM, Lemkes AH, Ruitenbeek W, et al. Mutation in mitochnodrial tRNA (Leu) (UUR) gene in a large pedigree with maternally transmitted type II DM and deafness[J]. Nature Genet, 1992, 1: 368-371.
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
Malecki MT, Jhala US, Antonellis A, et al. Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus[J]. Nat Genet, 1999, 23(3): 323-328.
Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q
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