Wolframin deficiency is accompanied with metabolic inflexibility in rat striated muscles

The protein wolframin is localized in the membrane of the endoplasmic reticulum (ER), influencing Ca2+ metabolism and ER interaction with mitochondria, but the exact role of the protein remains unclear. Mutations in Wfs1 gene cause autosomal recessive disorder Wolfram syndrome (WS). The first sympto...

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Detalles Bibliográficos
Autores principales: Tepp, Kersti, Aid-Vanakova, Jekaterina, Puurand, Marju, Timohhina, Natalja, Reinsalu, Leenu, Tein, Karin, Plaas, Mario, Shevchuk, Igor, Terasmaa, Anton, Kaambre, Tuuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918847/
https://www.ncbi.nlm.nih.gov/pubmed/35295995
http://dx.doi.org/10.1016/j.bbrep.2022.101250

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918847/
https://www.ncbi.nlm.nih.gov/pubmed/35295995
http://dx.doi.org/10.1016/j.bbrep.2022.101250

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