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Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P356
Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-67E11446-B665-4BC2-8813-1E7DC5B105DE
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2959da6c0cdb478c3ea5c9efa051ad41573efacb
P356
10.1002/HUMU.23186
http://www.w3.org/2001/XMLSchema#string
P356
HUMU.23186