Refine your search
Availability
-
Authors
-
Topics
- Adult
- Autoimmune Diseases
- Autoimmunity
- Congenital Hyperinsulinism
- Fatal Outcome
- Genes, Dominant
- Genotype
- Humans
- Immunoglobulins
- Infant
- Infant, Newborn
- Infant, Premature
- Islets of Langerhans
- Male
- Mutation
- Phenotype
- Protein Tyrosine Phosphatase, Non-Receptor Type 11
- Sulfonylurea Receptors
- blood
- genetics
- Show more
- Show less
-
Languages