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Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is a hereditary metabolic disease arising from biallelic mutations of SLC25A13. This study aimed to explore the characteristics of fasting blood glucose (FBG), fasting insulin (FINS) and C-peptide (C-P) levels in NICCD infants, an...
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| Publicado no: | Exp Biol Med (Maywood) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5476344/ https://ncbi.nlm.nih.gov/pubmed/28516797 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1535370217710918 |
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