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1750-1172-9-72
1750-1172-9-72
https://scigraph.springernature.com/pub.10.1186/1750-1172-9-72
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
P2888
1750-1172-9-72
https://scigraph.springernature.com/pub.10.1186/1750-1172-9-72