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Q42752301-2814C253-39EE-4EBA-9182-FEE4D9CC2F7D
Q42752301-2814C253-39EE-4EBA-9182-FEE4D9CC2F7D
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http://www.wikidata.org/entity/statement/Q42752301-2814C253-39EE-4EBA-9182-FEE4D9CC2F7D
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-2814C253-39EE-4EBA-9182-FEE4D9CC2F7D
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Statement
http://www.wikidata.org/entity/statement/Q42752301-2814C253-39EE-4EBA-9182-FEE4D9CC2F7D
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wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3.