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Q36580567-191D055C-F54B-46D7-A46E-D3D018572858
Q36580567-191D055C-F54B-46D7-A46E-D3D018572858
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http://www.wikidata.org/entity/statement/Q36580567-191D055C-F54B-46D7-A46E-D3D018572858
Correlated alterations in genome organization, histone methylation, and DNA-lamin A/C interactions in Hutchinson-Gilford progeria syndrome.
P2860
Q36580567-191D055C-F54B-46D7-A46E-D3D018572858
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36580567-191D055C-F54B-46D7-A46E-D3D018572858
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wasDerivedFrom
d7eed538547f7a62f4525d989702de0d08c76f9a
P2860
The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin