Incomplete processing of mutant lamin A in Hutchinson–Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition

Author： Glynn Michael W.   Glover Thomas W.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.14, Iss.20, 2005-10, pp. : 2959-2969

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