LE WE PMID CA
ABCC8 SUR110858ABCC8 SUR1

ABCC8 SUR1

ABCC9 SUR2A

ABCC9 SUR2B

Adrenergic atrial fibrillation

Anemia (megaloblastic thiamine responsive)

Beckwith Wiedemann syndrome

Bererdinelli Seip congenital lipodystrophy

BSCL1 AGPAT2

BSCL2 Seipin

Congenital hyperinsulinism

DEND syndrome

Diabetes mellitus (Hereditary MODY)

Diabetes mellitus (hereditary)

Diabetes mellitus (neonatal transient)

Diabetes mellitus (neonatal)

Donohue s syndrome Leprechaunism

EIF2AK3 PERK

FRDA1 Frataxin

Friedreich ataxia

Glucokinase

Glucose (Hypoglycemia)

GLUD1

Glutamate dehydrogenase

Heart (Cardiomyopathy dilated)

Hyperinsulinism in infancy

Insulin resistance type a

Ion channel (Potassium)

KATP

KCNJ11 Kir6 2

KCNJ8 Kir6 1

Lipodystrophy

OMIM_601487

OMIM_x600937

Perlman syndrome

Persistent hyperinsulinemic hypoglycemia of infancy

Persistent neonatal hypoglycemia

Rabson Mendenhall s syndrome

Receptor (Insulin)

Receptor (PPAR gamma)

Short chain L 3 hydroxyacyl CoA dehydrogenase

SLC19A2 THTR1

Sotos s syndrome

TNDM29locus

Werner s syndrome

Wfs1 Wolframin

Wfs2

Wolcott Rallison syndrome

Wolfram s syndrome DIDMOAD

WRN

2010  
1
Human K(ATP) channelopathies: diseases of metabolic homeostasis.
[20033705] Pflugers Arch 460(2): 295-306 (2010)
2010  
2
Cardiac sarcolemmal K(ATP) channels: Latest twists in a questing tale!
[19607836] J Mol Cell Cardiol 48(1): 71-5 (2010)
2006  
3
Molecular mechanisms of neonatal hyperinsulinism.
[17003566] Horm Res 66(6): 289-96 (2006)
2005  
4
Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.
[15772126] J Med Genet 42(12): 893-902 (2005)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.



  • ABCC8 SUR1

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