Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene
Abstract
Heterozygous loss-of-function mutations in the glucokinase (GCK) gene cause MODY 2, which is characterized by asymptomatic fasting hyperglycemia and does not require insulin treatment. Conversely, homozygous loss-of-function mutations in the same gene give rise to permanent neonatal diabetes mellitus (DM) that appears in the first 6-9 months of life and necessitates lifelong insulin treatment. We aimed to present the genotypic and phenotypic...
Paper Details
Title
Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene
Published Date
Oct 25, 2021
Journal
Volume
21
Issue
1
Pages
163 - 169
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