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Q34478016-69FDF05B-048A-4052-8914-88295A4B5E5B
Q34478016-69FDF05B-048A-4052-8914-88295A4B5E5B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478016-69FDF05B-048A-4052-8914-88295A4B5E5B
Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome.
P2860
Q34478016-69FDF05B-048A-4052-8914-88295A4B5E5B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478016-69FDF05B-048A-4052-8914-88295A4B5E5B
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wasDerivedFrom
3a80ede8d500c5294542c7d4815dd423fa868b1c
P2860
CEP152 is a genome maintenance protein disrupted in Seckel syndrome