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We describe a codon 299 mutation in the glucokinase gene in a British pedigree with maturity-onset diabetes of the young (MODY) resulting in a substitution of glycine to arginine. One out of fifty patients diagnosed with classical late-onset type 2 diabetes mellitus was also found to have this mutation. All nine relatives of this patient who have inherited the mutation have type 2 diabetes, although six others without the mutation are also present with diabetes. The discovery that glucokinase mutations can cause MODY and was also found in ten affected members of a pedigree with type 2 diabetes in which MODY had not previously been considered indicates that diagnosis based on molecular pathology will be helpful in understanding the aetiology of type 2 diabetes.

More information Original publication

DOI

10.1038/ng1092-153

Type

Journal article

Publication Date

1992-10-01T00:00:00+00:00

Volume

2

Pages

153 - 156

Total pages

3

Addresses

H, o, w, a, r, d, , H, u, g, h, e, s, , M, e, d, i, c, a, l, , I, n, s, t, i, t, u, t, e, ,, , U, n, i, v, e, r, s, i, t, y, , o, f, , C, h, i, c, a, g, o, ,, , I, l, l, i, n, o, i, s, , 6, 0, 6, 3, 7, .

Keywords

Humans, Diabetes Mellitus, Type 2, Glucokinase, DNA, Pedigree, DNA Mutational Analysis, Base Sequence, Phenotype, Point Mutation, Exons, Molecular Sequence Data, Adolescent, Adult, Aged, Middle Aged, Child, Female, Male