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A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes
Neonatal diabetes mellitus (NDM) is a rare type of monogenic diabetes that presents in the first 6 months of life. Activating mutations in the KCNJ11 gene encoding for the Kir6.2 subunit of the ATP-sensitive potassium (K(ATP) ) channel can lead to transient NDM (TNDM) or to permanent NDM (PNDM). A f...
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| Pubblicato in: | J Clin Res Pediatr Endocrinol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Galenos Publishing
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5985388/ https://ncbi.nlm.nih.gov/pubmed/28943514 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.5166 |
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