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Q38286122-310BFD20-CAE2-4103-869A-AC7D18225DEE
Q38286122-310BFD20-CAE2-4103-869A-AC7D18225DEE
BestRank
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http://www.wikidata.org/entity/statement/Q38286122-310BFD20-CAE2-4103-869A-AC7D18225DEE
Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk.
P2860
Q38286122-310BFD20-CAE2-4103-869A-AC7D18225DEE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38286122-310BFD20-CAE2-4103-869A-AC7D18225DEE
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wasDerivedFrom
f3de7f7b6cc0727b6964f86338ff2990a31fedf8
P2860
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.