Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia

BACKGROUND: Hyperinsulinaemic hypoglycaemia (HH) is a group of clinically and genetically heterogeneous disorders characterized by unregulated insulin secretion. Abnormalities in nine different genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A, UCP2 and HNF1A) have been reported in HH, the most...

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Veröffentlicht in:BMC Res Notes
Hauptverfasser: Senniappan, Senthil, Sadeghizadeh, Atefeh, Flanagan, Sarah E, Ellard, Sian, Hashemipour, Mahin, Hosseinzadeh, Majid, Salehi, Mansour, Hussain, Khalid
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2015
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Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4535259/
https://ncbi.nlm.nih.gov/pubmed/26268944
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1319-1
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