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Q51158820-9B4CA6FF-A739-48D8-8420-74DC6B697DB0
Q51158820-9B4CA6FF-A739-48D8-8420-74DC6B697DB0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-9B4CA6FF-A739-48D8-8420-74DC6B697DB0
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P1476
Q51158820-9B4CA6FF-A739-48D8-8420-74DC6B697DB0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-9B4CA6FF-A739-48D8-8420-74DC6B697DB0
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2959da6c0cdb478c3ea5c9efa051ad41573efacb
P1476
Filamin B Loss-of-Function Mut
......
s Syndrome with Rib Anomalies.
@en