Učitavanje...

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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Bibliografski detalji
Izdano u:Pediatr Diabetes
Glavni autori: Tung, Joanna Yuet-ling, Boodhansingh, Kara, Stanley, Charles A, De León, Diva D
Format: Artigo
Jezik:Inglês
Izdano: 2018
Teme:
Online pristup: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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