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For instance, patients with Wolfram Syndrome (WS) have rare autosomal recessive mutations in their WFS1 gene that give rise to multiple complications, such as juvenile-onset diabetes, optic atrophy, and deafness (185)
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[DOI] [PubMed] [Google Scholar] 11.Emmert S, Quargnali G, Thallmair S, Rivera-Fuentes P: A locally activatable sensor for robust quantification of organellar glutathione
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