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Clinical heterogeneity of hyperinsulinism due to HNF1A and HNF4A mutations
BACKGROUND: Dominant inactivating mutations in HNF1A and HNF4A have been described to cause hyperinsulinism (HI) before evolving to diabetes. However, information available in the literature regarding the clinical phenotype is limited. OBJECTIVE: To report the prevalence of HNF1A and HNF4A mutations...
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| Publicado en: | Pediatr Diabetes |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6030428/ https://ncbi.nlm.nih.gov/pubmed/29493090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pedi.12655 |
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