Neonatal diabetes mellitus due to a new KCNJ11 mutation - 10 years of the patient`s follow-up
Background. Mutations in the KCNJ11 gene, which encodes the Kir6.2 subunit of the ATP-sensitive potassium channel, often result in neonatal diabetes. Case. In this report, we describe a 10-year-old girl who is heterozygous for a new missense mutation in the KCNJ11 gene and whose treatm...
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| Principais autores: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Hacettepe University Institute of Child Health
2021-06-01
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| סדרה: | The Turkish Journal of Pediatrics |
| נושאים: | |
| גישה מקוונת: | https://turkjpediatr.org/article/view/323 |
| תגים: |
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