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Gigascience 6(6):033
Similar content being viewed by others Introduction One rare neurodegenerative disorder with an autosomal recessive inheritance pattern is Wolfram syndrome (WS), which is caused by biallelic mutations of the Wolframin ER transmembrane glycoprotein (Wfs1) gene and first manifests as diabetes mellitus, followed by optic nerve atrophy, deafness, and symptoms of neurodegeneration 1,2,3
Around six months in, he figured he was in the clear and, with his doctors consent, he stopped taking naltrexone completely
Is there a follow-up schedule built into the program (e.g., labs at 6 and 12 weeks for TRT)
A Penn State study showed Setria raised glutathione levels by 35% in red blood cells when taken orally
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