Hutchinson-Gilford progeria syndrome (HGPS) is a genetic disorder displaying features reminiscent of premature senescence caused by germline mutations in the LMNA gene encoding lamin A and C. essential components of the nuclear lamina. By studying a family with homozygous LMNA mutation (K542N). we showed that HGPS can also be caused by mutations affecting both isoforms. https://safeersappliancers.shop/product-category/bosch-cma585gs0b-serie-6-900-watt-microwave-built-in-stainless-steel/