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Q37185993-69E9E52B-3333-4095-BFB4-49AA009B6494
Q37185993-69E9E52B-3333-4095-BFB4-49AA009B6494
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http://www.wikidata.org/entity/statement/Q37185993-69E9E52B-3333-4095-BFB4-49AA009B6494
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
P2860
Q37185993-69E9E52B-3333-4095-BFB4-49AA009B6494
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37185993-69E9E52B-3333-4095-BFB4-49AA009B6494
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wasDerivedFrom
8555ed94f66d5ab508631223a31e0c45b389d00d
P2860
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium