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Q51158820-DFE70853-E82A-4FA6-B517-F6D2A396738D
Q51158820-DFE70853-E82A-4FA6-B517-F6D2A396738D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-DFE70853-E82A-4FA6-B517-F6D2A396738D
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-DFE70853-E82A-4FA6-B517-F6D2A396738D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-DFE70853-E82A-4FA6-B517-F6D2A396738D
rank
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type
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Statement
wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.