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Q51158820-1A6F3A02-B3E6-47DF-9F05-F44A15CCCA0C
Q51158820-1A6F3A02-B3E6-47DF-9F05-F44A15CCCA0C
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http://www.wikidata.org/entity/statement/Q51158820-1A6F3A02-B3E6-47DF-9F05-F44A15CCCA0C
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-1A6F3A02-B3E6-47DF-9F05-F44A15CCCA0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-1A6F3A02-B3E6-47DF-9F05-F44A15CCCA0C
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wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB