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Q33954902-AEF4918C-9156-4138-829D-EAEB41FAED69
Q33954902-AEF4918C-9156-4138-829D-EAEB41FAED69
BestRank
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http://www.wikidata.org/entity/statement/Q33954902-AEF4918C-9156-4138-829D-EAEB41FAED69
Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS).
P2860
Q33954902-AEF4918C-9156-4138-829D-EAEB41FAED69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33954902-AEF4918C-9156-4138-829D-EAEB41FAED69
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wasDerivedFrom
7984678ee1383d273f4f43d76c1a6df7deb1221b
P2860
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype