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Q24609805-2CCC62D0-0DD5-404F-B685-111F981E4ACE
Q24609805-2CCC62D0-0DD5-404F-B685-111F981E4ACE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24609805-2CCC62D0-0DD5-404F-B685-111F981E4ACE
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
P2860
Q24609805-2CCC62D0-0DD5-404F-B685-111F981E4ACE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24609805-2CCC62D0-0DD5-404F-B685-111F981E4ACE
rank
NormalRank
type
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wasDerivedFrom
d4e5aba8e6d14cbfe65fb545a5a81809e7ed4c5a
P2860
Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.