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KCNJ11 gene mutation
Clinical significance:
- KCNJ11 gene mutations are associated with
- neonatal diabetes mellitus
- familial hyperinsulinemic hypoglycemia type 2
Related
inwardly-rectifying K+ channel J11; ATP-sensitive inward rectifier K+ channel 11; K+ channel, inwardly rectifying subfamily J member 11; inward rectifier K+ channel Kir6.2; IKATP (KCNJ11)
General
gene mutation testing; gene mutation analysis
References
Loinc