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Q42752301-2FAD3682-C9EF-41B0-A69D-B74A941C91EC
Q42752301-2FAD3682-C9EF-41B0-A69D-B74A941C91EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-2FAD3682-C9EF-41B0-A69D-B74A941C91EC
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-2FAD3682-C9EF-41B0-A69D-B74A941C91EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-2FAD3682-C9EF-41B0-A69D-B74A941C91EC
rank
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type
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Statement
wasDerivedFrom
efef274949e84feb815cac728202756278a45a9a
P2860
Normal cognitive functions in joubert syndrome.