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Q47288069-338B460B-1E34-4619-B363-15E50FC915CA
Q47288069-338B460B-1E34-4619-B363-15E50FC915CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47288069-338B460B-1E34-4619-B363-15E50FC915CA
Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons.
P2860
Q47288069-338B460B-1E34-4619-B363-15E50FC915CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47288069-338B460B-1E34-4619-B363-15E50FC915CA
rank
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type
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Statement
wasDerivedFrom
a56ea0f8307d785d6ab1b22f3a66e4ab580d5d6b
P2860
Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism