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Q48788494-2671E732-F0E3-4BF2-A510-47F2EEB1C385
Q48788494-2671E732-F0E3-4BF2-A510-47F2EEB1C385
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http://www.wikidata.org/entity/statement/Q48788494-2671E732-F0E3-4BF2-A510-47F2EEB1C385
Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
P2860
Q48788494-2671E732-F0E3-4BF2-A510-47F2EEB1C385
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48788494-2671E732-F0E3-4BF2-A510-47F2EEB1C385
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wasDerivedFrom
93c4d3722b11180b9488ec35aa49ef338d0578cd
P2860
A novel whole exon deletion in WWOX gene causes early epilepsy, intellectual disability and optic atrophy.