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Novel heterozygous mutation c.4282G>T in the SCN5A gene in a family with Brugada syndrome
Brugada syndrome (BrS) is a rare, inherited arrhythmia syndrome. The most well-known gene that is responsible for causing BrS is SCN5A, which encodes the human cardiac Na(+) channel (Na(v)1.5) α subunit. To date, it has been reported that >100 mutations in SCN5A can cause BrS. In the present stud...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4471719/ https://ncbi.nlm.nih.gov/pubmed/26136871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2015.2361 |
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