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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Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea: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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