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Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features
Inwardly rectifying potassium channels (Kir channels) control cell membrane K(+) fluxes and electrical signaling in diverse cell types. Heterozygous mutations in the human Kir6.2 gene (KCNJ11), the pore-forming subunit of the ATP-sensitive (K(ATP)) channel, cause permanent neonatal diabetes mellitus...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC536014/ https://ncbi.nlm.nih.gov/pubmed/15583126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0404756101 |
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