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Q24676539-13B80E62-3270-4384-994B-702277CDBC1D
Q24676539-13B80E62-3270-4384-994B-702277CDBC1D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-13B80E62-3270-4384-994B-702277CDBC1D
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
P2093
Q24676539-13B80E62-3270-4384-994B-702277CDBC1D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-13B80E62-3270-4384-994B-702277CDBC1D
rank
NormalRank
type
BestRank
Statement
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
H L Wilson
http://www.w3.org/2001/XMLSchema#string