Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients

The autosomal recessive form of persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is associated with mutations in either ABCC8 or KCNJ11 genes. In the present study, we describe the clinical features and results of genetic analysis of 13 Saudi Arabian patients with PHHI. Clinically, most pa...

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Detalles Bibliográficos
Autores principales: Adi, Ahmad, Bin Abbas, Bassam, Al Hamed, Mohamed, Al Tassan, Nada, Bakheet, Dana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488661/
https://www.ncbi.nlm.nih.gov/pubmed/25871929
http://dx.doi.org/10.3390/genes6020206

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488661/
https://www.ncbi.nlm.nih.gov/pubmed/25871929
http://dx.doi.org/10.3390/genes6020206

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