Peroxisomal abnormalities and catalase deficiency in Hutchinson-Gilford Progeria Syndrome.Post author:caolab75@gmail.comPost published:March 31, 2020Post category:Articlesaging-12-102941 You Might Also Like Rapamycin reverses cellular phenotype and enhances mutant protein clearance in Hutchinson Gilford progeria syndrome. June 29, 2011 Mechanisms of genome instability in Hutchinson-Gilford progeria November 10, 2016 Phenotype-Dependent Coexpression Gene Clusters: Application to Normal and Premature Ageing January 2, 2015
Rapamycin reverses cellular phenotype and enhances mutant protein clearance in Hutchinson Gilford progeria syndrome. June 29, 2011
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