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Q33954902-7185EBFD-AC18-457B-AA72-7D6F4C89DC74
Q33954902-7185EBFD-AC18-457B-AA72-7D6F4C89DC74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33954902-7185EBFD-AC18-457B-AA72-7D6F4C89DC74
Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS).
P2860
Q33954902-7185EBFD-AC18-457B-AA72-7D6F4C89DC74
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33954902-7185EBFD-AC18-457B-AA72-7D6F4C89DC74
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wasDerivedFrom
7984678ee1383d273f4f43d76c1a6df7deb1221b
P2860
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification.