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Q51158820-17BED731-B5E9-4663-B35C-A630040659BE
Q51158820-17BED731-B5E9-4663-B35C-A630040659BE
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http://www.wikidata.org/entity/statement/Q51158820-17BED731-B5E9-4663-B35C-A630040659BE
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-17BED731-B5E9-4663-B35C-A630040659BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-17BED731-B5E9-4663-B35C-A630040659BE
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wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome.