Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism

OBJECTIVE: Congenital hyperinsulinism (CHI) is the most frequent cause of severe and persistent hypoglycaemia from birth. Understanding the pathophysiology and genetic defects behind hyperinsulinism and its complications provides clues to timely diagnosis and management. The aim of this study was to...

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Detalles Bibliográficos
Autores principales: Razzaghy-Azar, Maryam, Saeedi, Saeedeh, Dayani, Sepideh Borhan, Enayati, Samaneh, Abbasi, Farzaneh, Hashemian, Somayyeh, Eshraghi, Peyman, Karimdadi, Siroos, Tajdini, Parisa, Vakili, Rahim, Amoli, Mahsa M., Yaghootkar, Hanieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900073/
https://www.ncbi.nlm.nih.gov/pubmed/34927408
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2021.0071

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900073/
https://www.ncbi.nlm.nih.gov/pubmed/34927408
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2021.0071

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