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Q41928481-8CDCE44E-B0B2-42BB-B3CF-B457335F0D4D
Q41928481-8CDCE44E-B0B2-42BB-B3CF-B457335F0D4D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-8CDCE44E-B0B2-42BB-B3CF-B457335F0D4D
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P407
Q41928481-8CDCE44E-B0B2-42BB-B3CF-B457335F0D4D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-8CDCE44E-B0B2-42BB-B3CF-B457335F0D4D
rank
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type
BestRank
Statement
P407
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