Germline and somatic mutations in histologically atypical congenital hyperinsulinism
BackgroundIn histologically atypical congenital hyperinsulinism (CHI), correlations between clinical, histological and genetic features are largely unknown. Laser-capture microdissection may be used to identify low-grade mosaic DNA variants in the islets of Langerhans.AimTo investigate genotype-hist...
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| Autores principales: | , , , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Frontiers Media S.A.
2026-01-01
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| Colección: | Frontiers in Endocrinology |
| Materias: | |
| Acceso en línea: | https://www.frontiersin.org/articles/10.3389/fendo.2025.1692539/full |
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