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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Bibliografiske detaljer
Udgivet i:BMC Res Notes
Main Authors: Senniappan, Senthil, Sadeghizadeh, Atefeh, Flanagan, Sarah E, Ellard, Sian, Hashemipour, Mahin, Hosseinzadeh, Majid, Salehi, Mansour, Hussain, Khalid
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2015
Fag:
Research Article
Online adgang: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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