A carregar...
A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation
Missense mutations in the skeletal muscle sodium channel α-subunit gene (SCN4A) are associated with a group of clinically overlapping diseases caused by alterations in the excitability of the sarcolemma. Sodium channel defects may increase excitability and cause myotonic stiffness or may render fibr...
Na minha lista:
| Main Authors: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2005
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1464529/ https://ncbi.nlm.nih.gov/pubmed/15774523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2005.082909 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|