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The association between clinical phenotype of Parkinson’s disease and LRRK2 variants in China

2020-03-30

Abstract excerpt

<h4>Introduction: </h4> LRRK2 G2385R and LRRK2 S1647T have been identified as the most common risk variants for PD in the Chinese population. The aim of the study was to explore the correlation of LRRK2 G2385R, LRRK2 S1647T and their haplotypes with symptoms. <h4>Method:</h4> Demographic variables, disease-related variables and motor and non-motor assessments was collected in the study. Peripheral blood samples we...

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Literature Corpus work
e1134471-a78c-591f-b0fb-437183d4d12f
DOI
10.21203/rs.3.rs-19854/v1
Open publication

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The association between clinical phenotype of Parkinson’s disease and LRRK2 variants in ChinaDOI 10.21203/rs.3.rs-19854/v1
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