Mutations in the KCNJ11 gene, which encodes the Kir6.2 subunit of the pancreatic KATP channel, cause neonatal diabetes. KCNJ11 is also expressed in the brain, and ~ 20% of those affected have neurological features, which may include features suggestive of psychiatric disorder. No previous studies have systematically characterized the psychiatric morbidity in people with KCNJ11 neonatal diabetes. We aimed to characterize the types of psychiatric disorders present in children with KCNJ11 mutations, and explore their impact on families.Pre-print (immediately), accepted manuscript (12 month embargo
AIMS: Heterozygous activating mutations in KCNJ11, which encodes the Kir6.2 subunit of the pancreati...
Neonatal diabetes can either remit and hence be transient or else may be permanent. These two phenot...
We have recently shown that permanent neonatal diabetes can be caused by activating mutations in KCN...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
KCNJ11 encodes Kir6.2, the pore-forming subunit of the ATP-sensitive potassium channel present in br...
Heterozygous activating mutations in the gene encoding for the ATP-sensitive potassium channel subun...
AIMS/HYPOTHESIS: Heterozygous activating mutations in KCNJ11, which encodes the Kir6.2 subunit of th...
Neonatal diabetes can either remit and hence be transient or else may be permanent. These two phenot...
Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes...
This is the author accepted manuscript. The final version is available from American Diabetes Associ...
Neonatal diabetes mellitus (NDM) is a rare type of monogenic diabetes that presents in the first 6 m...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Mutations in the KCNJ11 gene are responsible for the majority of permanent neonatal diabetes mellitu...
Gain-of-function mutations of KCNJ11 can cause permanent neonatal diabetes mellitus, but only rarely...
Central nervous system (CNS) features in children with permanent neonatal diabetes (PNDM) due to KCN...
AIMS: Heterozygous activating mutations in KCNJ11, which encodes the Kir6.2 subunit of the pancreati...
Neonatal diabetes can either remit and hence be transient or else may be permanent. These two phenot...
We have recently shown that permanent neonatal diabetes can be caused by activating mutations in KCN...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
KCNJ11 encodes Kir6.2, the pore-forming subunit of the ATP-sensitive potassium channel present in br...
Heterozygous activating mutations in the gene encoding for the ATP-sensitive potassium channel subun...
AIMS/HYPOTHESIS: Heterozygous activating mutations in KCNJ11, which encodes the Kir6.2 subunit of th...
Neonatal diabetes can either remit and hence be transient or else may be permanent. These two phenot...
Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes...
This is the author accepted manuscript. The final version is available from American Diabetes Associ...
Neonatal diabetes mellitus (NDM) is a rare type of monogenic diabetes that presents in the first 6 m...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Mutations in the KCNJ11 gene are responsible for the majority of permanent neonatal diabetes mellitu...
Gain-of-function mutations of KCNJ11 can cause permanent neonatal diabetes mellitus, but only rarely...
Central nervous system (CNS) features in children with permanent neonatal diabetes (PNDM) due to KCN...
AIMS: Heterozygous activating mutations in KCNJ11, which encodes the Kir6.2 subunit of the pancreati...
Neonatal diabetes can either remit and hence be transient or else may be permanent. These two phenot...
We have recently shown that permanent neonatal diabetes can be caused by activating mutations in KCN...