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)),...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:ISRN Mol Biol
Main Authors: Leong, Ivone U. S., Skinner, Jonathan R., Shelling, Andrew N., Love, Donald R.
Formato: Artigo
Idioma:Inglês
Publicado: Hindawi Publishing Corporation 2013
Assuntos:
Research Article
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares