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Q21144407-2A3D241D-A33F-4015-A501-39395197CAED
Q21144407-2A3D241D-A33F-4015-A501-39395197CAED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21144407-2A3D241D-A33F-4015-A501-39395197CAED
The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin
P2860
Q21144407-2A3D241D-A33F-4015-A501-39395197CAED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21144407-2A3D241D-A33F-4015-A501-39395197CAED
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wasDerivedFrom
7831b4b5c406d439ed4183131638bb35c857307d
P2860
Structural organization of the human gene (LMNB1) encoding nuclear lamin B1