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Q36339758-D00F116A-E1FE-4001-BE7B-8B5F796C2E2D
Q36339758-D00F116A-E1FE-4001-BE7B-8B5F796C2E2D
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http://www.wikidata.org/entity/statement/Q36339758-D00F116A-E1FE-4001-BE7B-8B5F796C2E2D
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104
P2860
Q36339758-D00F116A-E1FE-4001-BE7B-8B5F796C2E2D
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Statement
http://www.wikidata.org/entity/statement/Q36339758-D00F116A-E1FE-4001-BE7B-8B5F796C2E2D
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8584cd4773617fd7d371515b852dd3fedd8fe1ce
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.