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Q51158820-0351C57B-3228-4610-AFE1-A10D0C9DC45C
Q51158820-0351C57B-3228-4610-AFE1-A10D0C9DC45C
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http://www.wikidata.org/entity/statement/Q51158820-0351C57B-3228-4610-AFE1-A10D0C9DC45C
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-0351C57B-3228-4610-AFE1-A10D0C9DC45C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-0351C57B-3228-4610-AFE1-A10D0C9DC45C
rank
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wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.