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...

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Detalles Bibliográficos
Autores principales: Horita, Shoichiro, Ono, Tomoyuki, Gonzalez-Resines, Saul, Ono, Yuko, Yamachi, Megumi, Zhao, Songji, Domene, Carmen, Maejima, Yuko, Shimomura, Kenju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
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

Internet

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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