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Q34393576-159C75F5-91C0-46AE-8655-DDDEFDBA40D6
Q34393576-159C75F5-91C0-46AE-8655-DDDEFDBA40D6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34393576-159C75F5-91C0-46AE-8655-DDDEFDBA40D6
Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans.
P2860
Q34393576-159C75F5-91C0-46AE-8655-DDDEFDBA40D6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34393576-159C75F5-91C0-46AE-8655-DDDEFDBA40D6
rank
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Statement
wasDerivedFrom
3b498bbbb477b0775598fd7b762e2e050ae312a3
P2860
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone