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Q22252904-9443D3F8-DFDA-4AE0-B6DC-2DED4A9E86D7
Q22252904-9443D3F8-DFDA-4AE0-B6DC-2DED4A9E86D7
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http://www.wikidata.org/entity/statement/Q22252904-9443D3F8-DFDA-4AE0-B6DC-2DED4A9E86D7
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
P2860
Q22252904-9443D3F8-DFDA-4AE0-B6DC-2DED4A9E86D7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22252904-9443D3F8-DFDA-4AE0-B6DC-2DED4A9E86D7
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wasDerivedFrom
f6768e2cf71b833b6de2da2dfdd17d3aef08af36
P2860
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.