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Q24337720-55784879-E763-4F3D-95D2-9EA61F8CEDED
Q24337720-55784879-E763-4F3D-95D2-9EA61F8CEDED
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Statement
http://www.wikidata.org/entity/statement/Q24337720-55784879-E763-4F3D-95D2-9EA61F8CEDED
Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3
P2860
Q24337720-55784879-E763-4F3D-95D2-9EA61F8CEDED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24337720-55784879-E763-4F3D-95D2-9EA61F8CEDED
rank
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type
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Statement
wasDerivedFrom
ffd0cf51f03a4e4afb62142c04c5a5ce594b39ac
P2860
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement