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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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| Publicado no: | BMC Res Notes |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | 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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