The potential presence of the highly similar paralogue gene KCNE1B blurs the genetic basis of KCNE1-LQTS patients
| Autor: | Polyxeni Gourzi, Dimitrios Degiannis, Malena P. Pantou |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2019 |
| Předmět: |
Genetics
Genome Genetic testing Sequence Homology Amino Acid Basis (linear algebra) Base Sequence Genome Human Gene Expression Profiling High-Throughput Nucleotide Sequencing Biology Polymorphism Single Nucleotide Long QT Syndrome Viewpoint Potassium Channels Voltage-Gated Correspondence Protein Isoforms Humans Amino Acid Sequence Gene Genetics (clinical) Pseudogenes |
| Zdroj: | Eur J Hum Genet European Journal of Human Genetics |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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