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Q51158820-130C50B7-9D0D-4F24-9EED-73C093307AC3
Q51158820-130C50B7-9D0D-4F24-9EED-73C093307AC3
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http://www.wikidata.org/entity/statement/Q51158820-130C50B7-9D0D-4F24-9EED-73C093307AC3
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-130C50B7-9D0D-4F24-9EED-73C093307AC3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-130C50B7-9D0D-4F24-9EED-73C093307AC3
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33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
The mouse notches up another success: understanding the causes of human vertebral malformation.