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Q24301630-C2A5F433-A576-491B-A758-8F47985430E6
Q24301630-C2A5F433-A576-491B-A758-8F47985430E6
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http://www.wikidata.org/entity/statement/Q24301630-C2A5F433-A576-491B-A758-8F47985430E6
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
P2860
Q24301630-C2A5F433-A576-491B-A758-8F47985430E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24301630-C2A5F433-A576-491B-A758-8F47985430E6
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wasDerivedFrom
ba3aa688618510b3436bbb3309188843201f5d65
P2860
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development