Abstract
Maturity-onset diabetes of the young (MODY) is an autosomal dominant form of early onset diabetes. The hepatocyte nuclear factor-1-beta (HNF1B) gene is responsible for MODY type 5 (MODY5) with distinctive clinical features, including pancreatic atrophy and renal disease. We herein report a Japanese case of young-onset diabetes with typical phenotypes of MODY5 and a novel heterozygous missense mutation (p.L145Q) in the HNF1B gene. The mutation was located in the Pit-Oct-Unc (POU)-specific domain, and the amino acid residue L145 was highly conserved among species. It is strongly suggested that this mutation explains the phenotypes of MODY5.
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Kato, T., Tanaka, D., Muro, S., Jambaljav, B., Mori, E., Yonemitsu, S., … Inagaki, N. (2018). A novel p.L145q mutation in the HNF1B gene in a case of maturity-onset diabetes of the young type 5 (MODY5). Internal Medicine, 57(14), 2035–2039. https://doi.org/10.2169/internalmedicine.9692-17
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