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There is also an ASO in development for genetic ALS caused by a mitochondrial protein mutation (Table 9)

Proprits antioxydantes

doi:10.1111/j.1365-313X.2007.03389.x

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Rare Diseases - Glutathione Synthase Deficiency Glutathione synthase deficiency, or proglutamicaciduria, is the most severe form of glutathione deficiency

It is an effective TG-reducing agent and remains the only lipid modifying drug to date that reduces cardiovascular mortality over and above statin therapy