EpilepsyGene: a genetic resource for genes and mutations related to epilepsy
Epilepsy is one of the most prevalent chronic neurological disorders, afflicting about 3.5–6.5 per 1000 children and 10.8 per 1000 elderly people. With intensive effort made during the last two decades, numerous genes and mutations have been published to be associated with the disease. An organized...
Main Authors: | Ran, Xia, Li, Jinchen, Shao, Qianzhi, Chen, Huiqian, Lin, Zhongdong, Sun, Zhong Sheng, Wu, Jinyu |
---|---|
Format: | Online |
Language: | English |
Published: |
Oxford University Press
2015
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384015/ |
Similar Items
-
Progressive myoclonus epilepsy associated with SACS gene mutations
by: Nascimento, Fábio A., et al.
Published: (2016) -
Genetics and epilepsy
by: Steinlein, Ortrud K.
Published: (2008) -
Management of Epilepsy in Resource-Limited Areas: Establishing an Epilepsy Surgery Program in Iran
by: Asadi-Pooya, Ali A, et al.
Published: (2014) -
From Genetics to Genomics of Epilepsy
by: Garofalo, Silvio, et al.
Published: (2012) -
Genetics of inherited human epilepsies
by: Gourfinkel-An, Isabelle, et al.
Published: (2001)