Case Report: New insights about clinical manifestations of patients with GCK genetic variants
GCK-MODY is a genetic condition characterized by alterations in the GCK gene, which can include several types of inactivating genetic variants - ranging from missense and nonsense variants, and splice site variants, to small and large deletions and insertions in the gene. This disorder primarily aff...
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| Principais autores: | , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Frontiers Media S.A.
2025-04-01
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| Serier: | Frontiers in Endocrinology |
| Fag: | |
| Online adgang: | https://www.frontiersin.org/articles/10.3389/fendo.2025.1549279/full |
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