Absence of Mutations in Exon 6 of the TARDBP Gene in 207 Chinese Patients with Sporadic Amyotrohic Lateral Sclerosis

Mutations in the TARDBP gene, which encodes the Tar DNA binding protein, have been shown to causes of both familial amyotrophic lateral sclerosis (FALS) and sporadic ALS (SALS). Recently, several novel TARDBP exon 6 mutants have been reported in patients with ALS in Europe and America but not in Asi...

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Detalles Bibliográficos
Autores principales: Ye, Cheng-hui, Lu, Xi-lin, Zheng, Min-ying, Zhen, Jun, Li, Zhi-Ping, Shi, Lei, Liu, Zhi-yong, Feng, Lu-yang, Pei, Zhong, Yao, Xiao-li
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/PMC3706600/
https://www.ncbi.nlm.nih.gov/pubmed/23874513
http://dx.doi.org/10.1371/journal.pone.0068106

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