Article
Pathogenicity of a glucokinase gene mutation and description of its clinical phenotype.
Pediatric diabetes - 1 Sept 2020
Hunter Janel D, Staton Hope, Constantacos Cathrine, Walsh Elizabeth T, Crudo David F
Abstract excerpt
Glucokinase gene (GCK) mutations comprise approximately 10% of cases of maturity-onset diabetes of the young (MODY). Over 800 different mutations in GCK have been reported in the Human Gene Mutation Database, the vast majority of which result in MODY type 2. The missense mutation p.Leu122Val is listed in that database as "disease-causing;" however, the National Center for Biotechnology Information ClinVar...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
