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Q37185993-0C4B72E6-A67A-4A2E-901B-427E66F211E4
Q37185993-0C4B72E6-A67A-4A2E-901B-427E66F211E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37185993-0C4B72E6-A67A-4A2E-901B-427E66F211E4
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
P2860
Q37185993-0C4B72E6-A67A-4A2E-901B-427E66F211E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37185993-0C4B72E6-A67A-4A2E-901B-427E66F211E4
rank
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type
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Statement
wasDerivedFrom
8555ed94f66d5ab508631223a31e0c45b389d00d
P2860
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse