טוען...
Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutation
Permanent neonatal diabetes mellitus refers to diabetes that occurs before the age of 6 months and persists through life. It is a rare disorder affecting one in 0.2-0.5 million live births. Mutations in the gene KCNJ11, encoding the subunit Kir6.2, and ABCC8, encoding SUR1 of the ATP-sensitive potas...
שמור ב:
| הוצא לאור ב: | Korean J Pediatr |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
The Korean Pediatric Society
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4573445/ https://ncbi.nlm.nih.gov/pubmed/26388896 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2015.58.8.309 |
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