Article
Absence of mutations in exon 6 of the TARDBP gene in 207 Chinese patients with sporadic amyotrohic lateral sclerosis.
PloS one - 1 Jan 2013
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
Abstract excerpt
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 Asia. To further examine the spectrum and frequency of TARDBP exon 6 mutations, we investigated their frequency in...
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