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The timeline for these individuals will be on the longest end of the spectrum, often requiring more than 8-12 weeks to see significant results

Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreichs ataxia

They will probably work on creating better GLP-1 and GIP receptor drugs that have fewer side effects, examining the effects of GIP in conjunction with GLP-1

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Both subcutaneous and visceral fat decreased significantly