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K(ATP) channel mutations in congenital hyperinsulinism: Progress and challenges towards mechanism-based therapies
Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycemia in infancy/childhood and is a serious condition associated with severe recurrent attacks of hypoglycemia due to dysregulated insulin secretion. Timely diagnosis and effective treatment are crucial to prevent severe...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086357/ https://www.ncbi.nlm.nih.gov/pubmed/37056678 http://dx.doi.org/10.3389/fendo.2023.1161117 |