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Expression of a Mutant kcnj2 Gene Transcript in Zebrafish
Long QT 7 syndrome (LQT7, also known as Andersen-Tawil syndrome) is a rare autosomal-dominant disorder that causes cardiac arrhythmias, periodic paralysis, and dysmorphic features. Mutations in the human KCNJ2 gene, which encodes for the subunit of the potassium inwardly-rectifying channel (I(K1)),...
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| Publicado no: | ISRN Mol Biol |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4890933/ https://ncbi.nlm.nih.gov/pubmed/27335675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/324839 |
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