Laddar...
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...
Sparad:
| I publikationen: | Rare Dis |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Taylor & Francis
2015
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588220/ https://ncbi.nlm.nih.gov/pubmed/26481773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2015.1012978 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|