Identification of genetic variants in a pedigree associated with epilepsy by using whole exome sequencing and whole genome sequencing

Identification of genetic variants in a pedigree associated with epilepsy by using whole exome sequencing and whole genome sequencing

Epilepsy is a common heterogeneous group of neurological disorders including electroencephalographic and brain imaging. We used whole exome sequencing and whole genome sequencing to identify variants in a pedigree associated with epilepsy. Cranium CT scan showed that the lateral right parietal lo...

Full description

Bibliographic Details
Main Authors: Qin-Qin Zhang, Zi-Hua Wang, Jun-Shi Zhang, Jun-Nan Guo, Xu-Hong Lin, Lei An
Format: Article
Language:English
Published: IMR Press 2021-06-01
Series:Journal of Integrative Neuroscience
Subjects:
epilepsy
variant
tsc2
sequencing
Online Access:https://jin.imrpress.com/fileup/1757-448X/PDF/1625014735190-397105063.pdf

Internet

https://jin.imrpress.com/fileup/1757-448X/PDF/1625014735190-397105063.pdf

Similar Items