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Mutant huntingtin (mtHtt), an important trigger and pathological feature of HD, is caused by abnormal CAG trinucleotide repeat in the huntingtin ( HTT ) gene, resulting in amplification of polyglutamine repeats in mtHtt (Tabrizi et al

Hepatic overexpression of hemopexin inhibits inflammation and vascular stasis in murine models of sickle cell disease

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