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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Detalles Bibliográficos
Autores principales: Leong, Ivone U. S., Skinner, Jonathan R., Shelling, Andrew N., Love, Donald R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890933/
https://www.ncbi.nlm.nih.gov/pubmed/27335675
http://dx.doi.org/10.1155/2013/324839

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890933/
https://www.ncbi.nlm.nih.gov/pubmed/27335675
http://dx.doi.org/10.1155/2013/324839

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