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Q35229875-23C6A1DC-1CBF-4240-86DB-32BC4E326893
Q35229875-23C6A1DC-1CBF-4240-86DB-32BC4E326893
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35229875-23C6A1DC-1CBF-4240-86DB-32BC4E326893
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome
P2860
Q35229875-23C6A1DC-1CBF-4240-86DB-32BC4E326893
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35229875-23C6A1DC-1CBF-4240-86DB-32BC4E326893
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wasDerivedFrom
9853f1bf60349036650af6193b89949e7e23ed3b
P2860
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.