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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Published in:BMC Res Notes
Main Authors: Senniappan, Senthil, Sadeghizadeh, Atefeh, Flanagan, Sarah E, Ellard, Sian, Hashemipour, Mahin, Hosseinzadeh, Majid, Salehi, Mansour, Hussain, Khalid
Format: Artigo
Language:Inglês
Published: BioMed Central 2015
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Research Article
Online Access: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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