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Publikováno v:
Mechanisms of ageing and development. 130(6)
Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare premature aging disorder caused by mutations in the gene LMNA, which encodes the nuclear matrix protein lamin A. Previous research has shown that the average telomere length in fibroblasts from HG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b36a28e8de1fbffffd8493b0c48e113
https://pubmed.ncbi.nlm.nih.gov/19428457
https://pubmed.ncbi.nlm.nih.gov/19428457
