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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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Bibliografiska uppgifter
I publikationen:Rare Dis
Huvudupphovsmän: Bellin, Milena, Greber, Boris
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
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