| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4345121 | Neuroscience Letters | 2011 | 6 Pages |
Abstract
⺠GEFS+ is a familial autosomal dominant condition characterized by genetic heterogeneity. ⺠Mutation in the majority of families with GEFS+ has not identified yet. ⺠The aim is to search for the gene responsible for GEFS+ in three Chinese families. ⺠No mutation was found in coding and noncoding regions of the four genes in three Chinese families. ⺠There are as yet undiscovered mechanisms underlying GEFS+.
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Authors
Hua Lin, Jingyun Li, Mengyang Wang, Zheng Wang, Yuping Wang, Liwen Wu,