Epileptic encephalopathy with continuous spike-and-wave during sleep maps to a homozygous truncating mutation in AMPA receptor component FRRS1L
- Clin Genet. 2016 Sep;90(3):282-3. doi: 10.1111/cge.12796.
Affiliations
- 1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
- 2. Department of Pediatrics, Armed Forces Hospital, Khamis Mushayt, Saudi Arabia.
- 3. Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
- 4. Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
PMID: 27239025
DOI: 10.1111/cge.12796