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Structure based analysis of K(ATP) channel with a DEND syndrome mutation in murine skeletal muscle
Developmental delay, epilepsy, and neonatal diabetes (DEND) syndrome, the most severe end of neonatal diabetes mellitus, is caused by mutation in the ATP-sensitive potassium (K(ATP)) channel. In addition to diabetes, DEND patients present muscle weakness as one of the symptoms, and although the musc...
Autores principales: | Horita, Shoichiro, Ono, Tomoyuki, Gonzalez-Resines, Saul, Ono, Yuko, Yamachi, Megumi, Zhao, Songji, Domene, Carmen, Maejima, Yuko, Shimomura, Kenju |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988048/ https://www.ncbi.nlm.nih.gov/pubmed/33758250 http://dx.doi.org/10.1038/s41598-021-86121-5 |
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