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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2012
Matèries:
Research
Accés en línia: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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