<i>KCNJ11</i>activating mutations in Italian patients with permanent neonatal diabetes
Permanent neonatal diabetes mellitus (PNDM) is a rare condition characterized by severe hyperglycemia constantly requiring insulin treatment from its onset. Complete deficiency of glucokinase (GCK) can cause PNDM; however, the genetic etiology is unknown in most PNDM patients. Recently, heterozygous...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| 格式: | Artigo |
| 语言: | 英语 |
| 出版: |
2004
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| 在线阅读: | https://doi.org/10.1002/humu.20124 |
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