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Q42752301-885BE498-1D0E-448C-BED5-0941EBF14BC3
Q42752301-885BE498-1D0E-448C-BED5-0941EBF14BC3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-885BE498-1D0E-448C-BED5-0941EBF14BC3
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-885BE498-1D0E-448C-BED5-0941EBF14BC3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-885BE498-1D0E-448C-BED5-0941EBF14BC3
rank
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type
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wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome