Human iPS cell models of Jervell and Lange-Nielsen syndrome

Recessive mutations in the ion channel-encoding KCNQ1 gene may cause Jervell and Lange-Nielsen syndrome (JLNS), a fatal cardiac disease leading to arrhythmia and sudden cardiac death in young patients. Mutations in KCNQ1 may also cause a milder and dominantly inherited form of the disease, long QT s...

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Detalles Bibliográficos
Autores principales: Bellin, Milena, Greber, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588220/
https://www.ncbi.nlm.nih.gov/pubmed/26481773
http://dx.doi.org/10.1080/21675511.2015.1012978

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588220/
https://www.ncbi.nlm.nih.gov/pubmed/26481773
http://dx.doi.org/10.1080/21675511.2015.1012978

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