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Q34088135-7F6CC97F-B343-4A8A-86C6-4EC368576CE0
Q34088135-7F6CC97F-B343-4A8A-86C6-4EC368576CE0
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http://www.wikidata.org/entity/statement/Q34088135-7F6CC97F-B343-4A8A-86C6-4EC368576CE0
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.
P2860
Q34088135-7F6CC97F-B343-4A8A-86C6-4EC368576CE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34088135-7F6CC97F-B343-4A8A-86C6-4EC368576CE0
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wasDerivedFrom
a5f67a0fcd97a985c676bba90c498b1225ec627d
P2860
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue.