题名: A role for the Werner syndrome protein in epigenetic inactivation of the pluripotency factor Oct4
摘要: Abstract: Werner syndrome (WS) is an autosomal recessive disorder, the hallmarks of which are premature aging and early onset of neoplastic diseases (Orren, 2006; Bohr, 2008). The gene, whose mutation underlies the WS phenotype, is called WRN. The pr...

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