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Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism
CONTEXT: Hypoglycemia due to congenital hyperinsulinism (HI) is caused by mutations in 9 genes. OBJECTIVE: Our objective was to correlate genotype with phenotype in 417 children with HI. METHODS: Mutation analysis was carried out for the ATP-sensitive potassium (KATP) channel genes (ABCC8 and KCNJ11...
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| Hlavní autoři: | , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Endocrine Society
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3565119/ https://ncbi.nlm.nih.gov/pubmed/23275527 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2012-2169 |
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