Related Experiment Video
Updated: Oct 5, 2025
09:34
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
34.1K
A Rare Case of 3:1 Alpha Variant
1Department of Neurology, Seoul National University Hospital, Seoul, Korea.
Journal of Epilepsy Research
|January 28, 2022
Abstract:
Since the first documentation of slow alpha variants in Goodwin et al., there has been a single case report with an actual electroencephalography (EEG). However, any further case has not been reported since then, and neurologists are still unfamiliar with its presence due to its scarcity. Here, we present a rare case of 3:1 subharmonic alpha variant in a hope to acquaint EEG interpretations and speculate upon its benign nature.
Related Concept Videos
01:05Single Nucleotide Polymorphisms-SNPs
16.6K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
16.6K
01:49Multiple Allele Traits
35.7K
The Concept of Multiple Allelism
35.7K