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Association of Nurr1 gene mutations with Parkinson's disease in the Han population living in the Hubei province of China☆
Nurr1 defects could in part underlie Parkinson's disease pathogenesis, and Nurr1 gene polymorphism has been found in Caucasian patients with Parkinson's disease. In this study, heteroduplex technology was applied to compare the DNA sequences of eight exons of Nurr1 among 200 sporadic Parki...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302528/ https://www.ncbi.nlm.nih.gov/pubmed/25624803 http://dx.doi.org/10.3969/j.issn.1673-5374.2012.23.005 |