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Q36890893-6F8C8113-C798-4773-91BD-F42A95029E54
Q36890893-6F8C8113-C798-4773-91BD-F42A95029E54
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36890893-6F8C8113-C798-4773-91BD-F42A95029E54
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
P2860
Q36890893-6F8C8113-C798-4773-91BD-F42A95029E54
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36890893-6F8C8113-C798-4773-91BD-F42A95029E54
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wasDerivedFrom
561726a26027e5eaba28a1a0757ddadb04ea50be
P2860
Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.