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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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Publicado en:Pediatr Diabetes
Main Authors: Tung, Joanna Yuet-ling, Boodhansingh, Kara, Stanley, Charles A, De León, Diva D
Formato: Artigo
Idioma:Inglês
Publicado: 2018
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Acceso en liña: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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