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Q35394882-CB5A2925-9A57-4A15-ACEF-B5BF22FD6CB2
Q35394882-CB5A2925-9A57-4A15-ACEF-B5BF22FD6CB2
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http://www.wikidata.org/entity/statement/Q35394882-CB5A2925-9A57-4A15-ACEF-B5BF22FD6CB2
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.
P2860
Q35394882-CB5A2925-9A57-4A15-ACEF-B5BF22FD6CB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35394882-CB5A2925-9A57-4A15-ACEF-B5BF22FD6CB2
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wasDerivedFrom
3eb068ae52541ae9536a3328fffe138e813a6100
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.