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A novel mutation KCNJ11 R136C caused KCNJ11-MODY

Role of the KCNJ Gene Variants in the Clinical Outcome of Type 1 Diabetes

KCNJ11 downregulation stimulates cardiac cell apoptosis in myocarditis

Congenital Hyperinsulinism: A Novel Mutation in the KCNJ11 Gene

Precision medicine in KCNJ11 permanent neonatal diabetes

Genetic Screening for ABCC8 and KCNJ11 Polymorphisms among Arab Neonates

A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes

Normal expression of KCNJ11 is maintained by the G-quadruplex

DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea

Cognitive, Neurological, and Behavioral Features in Adults With KCNJ11 Neonatal Diabetes

The E23K Polymorphism of KCNJ11 and Diabetic Retinopathy in Northern Iran

ADHD, learning difficulties and sleep disturbances associated with KCNJ11-related neonatal diabetes

Neuropsychological impairments in children with KCNJ11 neonatal diabetes

Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?

Focal congenital hyperinsulinism resulting from biallelic loss of function of KCNJ11 gene

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