Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia

Autosomal recessive cerebellar ataxias are a group of neurodegenerative disorders that are characterized by complex clinical and genetic heterogeneity. Although more than 20 disease-causing genes have been identified, many patients are still currently without a molecular diagnosis. In a two-generati...

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Detalles Bibliográficos
Autores principales: Shi, Yuting, Wang, Junling, Li, Jia-Da, Ren, Haigang, Guan, Wenjuan, He, Miao, Yan, Weiqian, Zhou, Ying, Hu, Zhengmao, Zhang, Jianguo, Xiao, Jingjing, Su, Zheng, Dai, Meizhi, Wang, Jun, Jiang, Hong, Guo, Jifeng, Zhou, Yafang, Zhang, Fufeng, Li, Nan, Du, Juan, Xu, Qian, Hu, Yacen, Pan, Qian, Shen, Lu, Wang, Guanghui, Xia, Kun, Zhang, Zhuohua, Tang, Beisha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846781/
https://www.ncbi.nlm.nih.gov/pubmed/24312598
http://dx.doi.org/10.1371/journal.pone.0081884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846781/
https://www.ncbi.nlm.nih.gov/pubmed/24312598
http://dx.doi.org/10.1371/journal.pone.0081884

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