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Q42752301-1D437455-AE58-41E2-9959-D3E75B018FA1
Q42752301-1D437455-AE58-41E2-9959-D3E75B018FA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-1D437455-AE58-41E2-9959-D3E75B018FA1
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2888
Q42752301-1D437455-AE58-41E2-9959-D3E75B018FA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-1D437455-AE58-41E2-9959-D3E75B018FA1
rank
NormalRank
type
BestRank
Statement
P2888
1750-1172-9-72