valine has been researched along with Brugada Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Antzelevitch, C; Barajas-Martinez, H; Brugada, J; Brugada, P; Brugada, R; Burashnikov, E; Cordeiro, JM; Dumaine, R; Hong, K; Hu, D; Orsino, AM; Pfeiffer, R; Wu, YS | 1 |
1 other study(ies) available for valine and Brugada Syndrome
Article | Year |
---|---|
Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome.
Topics: Brugada Syndrome; Genetic Carrier Screening; Humans; Isoleucine; Leucine; Muscle Proteins; Mutation; NAV1.5 Voltage-Gated Sodium Channel; Pedigree; Phenotype; Proline; Sodium Channels; Valine | 2006 |