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Q33925250-57DAEE74-FC16-4E3C-A4A7-0E70F26231B4
Q33925250-57DAEE74-FC16-4E3C-A4A7-0E70F26231B4
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Statement
http://www.wikidata.org/entity/statement/Q33925250-57DAEE74-FC16-4E3C-A4A7-0E70F26231B4
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder
P2860
Q33925250-57DAEE74-FC16-4E3C-A4A7-0E70F26231B4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33925250-57DAEE74-FC16-4E3C-A4A7-0E70F26231B4
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aaaa1f069525f1513426b959763435bc43b3df38
P2860
Individual common variants exert weak effects on the risk for autism spectrum disorders