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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:BMC Res Notes
Prif Awduron: Senniappan, Senthil, Sadeghizadeh, Atefeh, Flanagan, Sarah E, Ellard, Sian, Hashemipour, Mahin, Hosseinzadeh, Majid, Salehi, Mansour, Hussain, Khalid
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2015
Pynciau:
Research Article
Mynediad Ar-lein: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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