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Q24676539-AE6BD15A-8CBC-4D21-93D2-1277EF2FE844
Q24676539-AE6BD15A-8CBC-4D21-93D2-1277EF2FE844
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http://www.wikidata.org/entity/statement/Q24676539-AE6BD15A-8CBC-4D21-93D2-1277EF2FE844
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
P2860
Q24676539-AE6BD15A-8CBC-4D21-93D2-1277EF2FE844
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-AE6BD15A-8CBC-4D21-93D2-1277EF2FE844
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wasDerivedFrom
e9ee99f938ee876c4d0f5805830d451363d2a72f
P2860
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.