KATP 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...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2023-03-01
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| Sarja: | Frontiers in Endocrinology |
| Aiheet: | |
| Linkit: | https://www.frontiersin.org/articles/10.3389/fendo.2023.1161117/full |
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