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Combined knockout of <i>Lrrk2</i> and <i>Rab29</i> does not result in behavioral abnormalities <i>in vivo</i>

2020-05-15

Abstract excerpt

Coding mutations in the LRRK2 gene, encoding for a large protein kinase, have been shown to cause familial Parkinson’s disease (PD). The immediate biological consequence of LRRK2 mutations is to increase kinase activity, leading to the suggestion that inhibition of this enzyme might be useful therapeutically to slow disease progression. Genome-wide association studies have identified the chromosomal loci around...

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Literature Corpus work
8c4431b7-92e9-59d1-81d0-c75b0c2312df
DOI
10.1101/2020.05.13.093708
Open publication

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Combined knockout of <i>Lrrk2</i> and <i>Rab29</i> does not result in behavioral abnormalities <i>in vivo</i>DOI 10.1101/2020.05.13.093708
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