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Q37195015-DFEA27D6-CC4B-452B-82FB-83492B0E8B8F
Q37195015-DFEA27D6-CC4B-452B-82FB-83492B0E8B8F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37195015-DFEA27D6-CC4B-452B-82FB-83492B0E8B8F
Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews
P2860
Q37195015-DFEA27D6-CC4B-452B-82FB-83492B0E8B8F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37195015-DFEA27D6-CC4B-452B-82FB-83492B0E8B8F
rank
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type
BestRank
Statement
wasDerivedFrom
872f09660894e8f579e15d3826148a74490b5422
P2860
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders