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Mutations in the ABHD5 gene result in the lipid storage myopathy (LSM) identified as neutral lipid storage disease with ichthyosis, NLSDI, also known as Chanarin-Dorfman syndrome
They also recently expanded into longevity treatments including NAD+ and sermorelin, though GLP-1 medications remain their bread and butter
The accumulation of hydrogen and lipid peroxides can damage liver cells and exacerbate the disease
Label each vial with the compound name, concentration, and reconstitution date
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