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Q24338649-8536388E-3702-4E9E-BE3E-C37A02D06F22
Q24338649-8536388E-3702-4E9E-BE3E-C37A02D06F22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338649-8536388E-3702-4E9E-BE3E-C37A02D06F22
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
P2860
Q24338649-8536388E-3702-4E9E-BE3E-C37A02D06F22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338649-8536388E-3702-4E9E-BE3E-C37A02D06F22
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Statement
wasDerivedFrom
f48e6e22b86aa5c270433579e08e89fdfdb842c3
P2860
A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus