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Q42752301-1E56AAB8-A0FE-416D-80EB-41D1940B5A3B
Q42752301-1E56AAB8-A0FE-416D-80EB-41D1940B5A3B
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http://www.wikidata.org/entity/statement/Q42752301-1E56AAB8-A0FE-416D-80EB-41D1940B5A3B
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-1E56AAB8-A0FE-416D-80EB-41D1940B5A3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-1E56AAB8-A0FE-416D-80EB-41D1940B5A3B
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wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome