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Q51158820-2583905C-D47A-4F5A-ADF2-09551F5039B6
Q51158820-2583905C-D47A-4F5A-ADF2-09551F5039B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-2583905C-D47A-4F5A-ADF2-09551F5039B6
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P1433
Q51158820-2583905C-D47A-4F5A-ADF2-09551F5039B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-2583905C-D47A-4F5A-ADF2-09551F5039B6
rank
NormalRank
type
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Statement
wasDerivedFrom
2959da6c0cdb478c3ea5c9efa051ad41573efacb
P1433
Human Mutation