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Maturity-Onset Diabetes of the Young: What Do Clinicians Need to Know?Undiagnosed MODY: Time for ActionWhole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.Genetic Counseling for Diabetes Mellitus.ABCC5 transporter is a novel type 2 diabetes susceptibility gene in European and African American populations.Exome sequencing and genetic testing for MODY.ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes.Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes.Molecular diagnosis of maturity onset diabetes of the young in India.Monogenic diabetes: a diagnostic algorithm for cliniciansEvaluation of a target region capture sequencing platform using monogenic diabetes as a study-model.Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study.Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.Comparative review of dipeptidyl peptidase-4 inhibitors and sulphonylureas.Complex Genetics of Type 2 Diabetes and Effect Size: What have We Learned from Isolated Populations?Pdx1 and USF transcription factors co-ordinately regulate Alx3 gene expression in pancreatic β-cells.Genetic Factors of Diabetes.Neonatal Diabetes and the KATP Channel: From Mutation to Therapy.Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention.A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family.A case of transient neonatal diabetes due to a novel mutation in ABCC8.Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemia.Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals.Functional and association analysis of an Amerindian-derived population-specific p.(Thr280Met) variant in RBPJL, a component of the PTF1 complex.Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.Mutations in HNF1A Gene are not a Common Cause of Familial Young-Onset Diabetes in Iran.Glucokinase mutations in pediatric patients with impaired fasting glucose.Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives.
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description
im Oktober 2011 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 12 October 2011
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 2011
@uk
name
Heterozygous ABCC8 mutations are a cause of MODY
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Heterozygous ABCC8 mutations are a cause of MODY
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type
label
Heterozygous ABCC8 mutations are a cause of MODY
@en
Heterozygous ABCC8 mutations are a cause of MODY
@nl
prefLabel
Heterozygous ABCC8 mutations are a cause of MODY
@en
Heterozygous ABCC8 mutations are a cause of MODY
@nl
P2093
P2860
P1433
P1476
Heterozygous ABCC8 mutations are a cause of MODY
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P2093
A T Hattersley
E L Edghill
M H Shepherd
P2860
P2888
P304
P356
10.1007/S00125-011-2319-X
P577
2011-10-12T00:00:00Z