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Q21144407-2077FE10-50F4-4317-9EF4-D29C7FFC20B2
Q21144407-2077FE10-50F4-4317-9EF4-D29C7FFC20B2
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http://www.wikidata.org/entity/statement/Q21144407-2077FE10-50F4-4317-9EF4-D29C7FFC20B2
The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin
P2860
Q21144407-2077FE10-50F4-4317-9EF4-D29C7FFC20B2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21144407-2077FE10-50F4-4317-9EF4-D29C7FFC20B2
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7831b4b5c406d439ed4183131638bb35c857307d
P2860
Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress