Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease.
Chunyu LiJunyu LinQirui JiangHui Fang ShangPublished in: European journal of neurology (2022)
Our study explored the rare variant of PLXNA1 in PD, and paves the way for future research on the genetic role of PLXNA1 in PD.
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