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Q47288069-E96382C5-3035-4CC2-89ED-6BE1F1D65846
Q47288069-E96382C5-3035-4CC2-89ED-6BE1F1D65846
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Statement
http://www.wikidata.org/entity/statement/Q47288069-E96382C5-3035-4CC2-89ED-6BE1F1D65846
Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons.
P2860
Q47288069-E96382C5-3035-4CC2-89ED-6BE1F1D65846
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47288069-E96382C5-3035-4CC2-89ED-6BE1F1D65846
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wasDerivedFrom
a56ea0f8307d785d6ab1b22f3a66e4ab580d5d6b
P2860
Pathogenic LRRK2 mutations, through increased kinase activity, produce enlarged lysosomes with reduced degradative capacity and increase ATP13A2 expression.