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Q35097630-1DF0A896-6A9C-429E-A473-143063B73859
Q35097630-1DF0A896-6A9C-429E-A473-143063B73859
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35097630-1DF0A896-6A9C-429E-A473-143063B73859
Genetic inactivation of ERK1 and ERK2 in chondrocytes promotes bone growth and enlarges the spinal canal
P2860
Q35097630-1DF0A896-6A9C-429E-A473-143063B73859
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35097630-1DF0A896-6A9C-429E-A473-143063B73859
rank
NormalRank
type
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Statement
wasDerivedFrom
f40619844da39cd94353d8ed61b01c1fe981f277
P2860
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome