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Q33608779-83B8CAB3-8ED9-42AC-A850-58F7D93F0AFA
Q33608779-83B8CAB3-8ED9-42AC-A850-58F7D93F0AFA
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Statement
http://www.wikidata.org/entity/statement/Q33608779-83B8CAB3-8ED9-42AC-A850-58F7D93F0AFA
Defective lamin A-Rb signaling in Hutchinson-Gilford Progeria Syndrome and reversal by farnesyltransferase inhibition.
P2860
Q33608779-83B8CAB3-8ED9-42AC-A850-58F7D93F0AFA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33608779-83B8CAB3-8ED9-42AC-A850-58F7D93F0AFA
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wasDerivedFrom
4956f25a55eb046892aa1b6c69d1f7ea0025d0a4
P2860
The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin