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Q51158820-D89816FF-2155-4CDA-BDC0-87221A58522E
Q51158820-D89816FF-2155-4CDA-BDC0-87221A58522E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-D89816FF-2155-4CDA-BDC0-87221A58522E
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P31
Q51158820-D89816FF-2155-4CDA-BDC0-87221A58522E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-D89816FF-2155-4CDA-BDC0-87221A58522E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2959da6c0cdb478c3ea5c9efa051ad41573efacb
P31
scholarly article