Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease
Movement Disorders, ISSN: 0885-3185, Vol: 26, Issue: 9, Page: 1729-1732
2011
- 22Citations
- 17Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations22
- Citation Indexes22
- 22
- CrossRef17
- Captures17
- Readers17
- 17
Article Description
Background:: Paired-like homodomain transcription factor 3 has been found to be important for the differentiation and survival of midbrain dopaminergic neurons. Methods:: To determine whether genetic variation in the coding region of the paired-like homodomain transcription factor 3 gene plays a role in Parkinson's disease, genetic analysis was performed in 112 patients with Parkinson's disease. Results:: We did not identify any mutations except rs2281983, but when we extended the analysis of rs2281983 and 2 intron variants (rs4919621 and rs3758549) in 336 patients with Parkinson's disease and 244 controls, we found that rs2281983 and rs4919621 appeared to confer susceptibility to Parkinson's disease, especially in early-onset Parkinson's disease and familial Parkinson's disease. © 2011 Movement Disorder Society.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79961208289&origin=inward; http://dx.doi.org/10.1002/mds.23693; http://www.ncbi.nlm.nih.gov/pubmed/21469209; https://onlinelibrary.wiley.com/doi/10.1002/mds.23693; https://dx.doi.org/10.1002/mds.23693; https://movementdisorders.onlinelibrary.wiley.com/doi/10.1002/mds.23693
Wiley
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