Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients

Significant advances in our understanding of the molecular mechanisms that cause congenital long QT syndrome (LQTS) have been made. A wide variety of experimental approaches, including heterologous expression of mutant ion channel proteins and the use of inducible pluripotent stem cell-derived cardi...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Biomolecules
Prif Awduron: Ono, Makoto, Burgess, Don E., Schroder, Elizabeth A., Elayi, Claude S., Anderson, Corey L., January, Craig T., Sun, Bin, Immadisetty, Kalyan, Kekenes-Huskey, Peter M., Delisle, Brian P.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2020
Pynciau:
Review
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7464307/
https://ncbi.nlm.nih.gov/pubmed/32759882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom10081144
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