Article

Low-frequency and rare coding variants of NUS1 contribute to pathogenesis and phenotype of Parkinson’s disease: a case-control study

2020-08-04

Abstract excerpt

<title>Abstract</title> Background NUS1 has recently been identified as a candidate risk gene for Parkinson’s disease (PD), but the contribution of NUS1 rare and low-frequency variants to PD susceptibility and phenotypes is largely unknown. Methods In our case-control study, whole-exome or Sanger sequencing was performed on the subjects (4,779 cases vs. 4,442 controls) to analyze the coding sequence of NUS1...

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Literature Corpus work: 37c87026-b061-55e2-9389-d547bd7f0514
DOI: 10.21203/rs.3.rs-51745/v1

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