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Q42752301-750A6424-848B-40DC-AB3B-C00EFE060EE0
Q42752301-750A6424-848B-40DC-AB3B-C00EFE060EE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-750A6424-848B-40DC-AB3B-C00EFE060EE0
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-750A6424-848B-40DC-AB3B-C00EFE060EE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-750A6424-848B-40DC-AB3B-C00EFE060EE0
rank
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type
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Statement
wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
Joubert syndrome: congenital cerebellar ataxia with the molar tooth