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Q28543099-6C2B4B2C-BDF0-4124-B511-D6F0D93F0FD0
Q28543099-6C2B4B2C-BDF0-4124-B511-D6F0D93F0FD0
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http://www.wikidata.org/entity/statement/Q28543099-6C2B4B2C-BDF0-4124-B511-D6F0D93F0FD0
Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients
P2860
Q28543099-6C2B4B2C-BDF0-4124-B511-D6F0D93F0FD0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28543099-6C2B4B2C-BDF0-4124-B511-D6F0D93F0FD0
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wasDerivedFrom
26af673aacdf5e03923f7a2d8f2e833089caae30
P2860
Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype-phenotype correlations