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Q28822028-DF289C5B-FDBC-451C-8DF5-A664D68C2887
Q28822028-DF289C5B-FDBC-451C-8DF5-A664D68C2887
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http://www.wikidata.org/entity/statement/Q28822028-DF289C5B-FDBC-451C-8DF5-A664D68C2887
Interruption of progerin-lamin A/C binding ameliorates Hutchinson-Gilford progeria syndrome phenotype
P2860
Q28822028-DF289C5B-FDBC-451C-8DF5-A664D68C2887
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28822028-DF289C5B-FDBC-451C-8DF5-A664D68C2887
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wasDerivedFrom
f85bbab8bb1d84f9da262a0e7c67a8dffde96a5a
P2860
The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin