Glucocerebrosidase L444P mutation confers genetic risk for Parkinson’s disease in central China

BACKGROUND: Mutations of the glucocerebrosidase (GBA) gene have reportedly been associated with Parkinson disease (PD) in various ethnic populations such as Singaporean, Japanese, Formosan, Canadian, American, Portuguese, Greek, Brazilian, British, Italian, Ashkenazi Jewish, southern and southwester...

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Dettagli Bibliografici
Autori principali: Wang, Youpei, Liu, Ling, Xiong, Jing, Zhang, Xiaowei, Chen, Zhenzhen, Yu, Lan, Chen, Chunnuan, Huang, Jinsha, Zhang, Zhentao, Mohmed, Asrah A, Lin, Zhicheng, Xiong, Nian, Wang, Tao
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2012
Soggetti:
Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3538614/
https://ncbi.nlm.nih.gov/pubmed/23227814
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-8-57
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