Monogenic diabetes, renal dysplasia and hypopituitarism: a patient with a HNF1A mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/qjmed/article-pdf/104/10/881/4513373/hcq195.pdf
Reference13 articles.
1. Clinical implications of a molecular genetic classification of monogenic β-cell diabetes
2. A 2-yr national population study of pediatric ketoacidosis in Sweden: predisposing conditions and insulin pump use
3. Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the young
4. Laron Dwarfism and Non-Insulin-Dependent Diabetes Mellitus in the Hnf-1 α Knockout Mouse
5. Hepatocyte Nuclear Factor 1 Inactivation Results in Hepatic Dysfunction, Phenylketonuria, and Renal Fanconi Syndrome
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1. Insights into the Genetics and Signaling Pathways in Maturity-Onset Diabetes of the Young;International Journal of Molecular Sciences;2022-10-26
2. HNF1A Mutations and Beta Cell Dysfunction in Diabetes;International Journal of Molecular Sciences;2022-03-16
3. Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders;The Journal of Clinical Endocrinology & Metabolism;2021-03-17
4. The Mutation Spectrum of Maturity Onset Diabetes of the Young (MODY)-Associated Genes among Western Siberia Patients;Journal of Personalized Medicine;2021-01-18
5. The molecular functions of hepatocyte nuclear factors – In and beyond the liver;Journal of Hepatology;2018-05
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