autosomal recessive hyperinsulinism due to Kir6.2 deficiency (Q56014286)
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human disease
- Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive hyperinsulinism due to Kir6.2 deficiency |
human disease |
|
Statements
Identifiers
1 reference
1 reference