Atomic-level investigation of KCNJ2 mutations associated with ventricular arrhythmic syndrome phenotypes
Abstract KCNJ2 encodes the inward rectifying potassium channel (Kir2.1) that underlies I K1 which maintains the cardiac resting membrane potential and regulates excitability. Mutations in KCNJ2 have been linked to several clinical phenotypes associated with life-threatening ventricular arrhythmia an...
Saved in:
| Main Authors: | Saba Munawar, Corey L. Anderson, Louise Reilly, Ryan Woltz, Yusra Sajid Kiani, Nipavan Chiamvimonvat, Lee L. Eckhardt |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-04-01
|
| Series: | Scientific Reports |
| Subjects: | |
| Online Access: | https://doi.org/10.1038/s41598-025-95062-2 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Dynamic duo: Kir6 and SUR in KATP channel structure and function
by: Bruce L. Patton, et al.
Published: (2024-12-01) -
Astrocytic proteins involved in regulation of the extracellular environment are increased in the Alzheimer's disease middle temporal gyrus
by: Henry Liu, et al.
Published: (2025-01-01) -
Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism?
by: Ayşe Balat, et al.
Published: (2020-04-01) -
Gestasyonel diyabet gelişiminde KCNJ11 geninin rolü
by: Funda İşcioğlu, et al.
Published: (2015-12-01) -
Challenges in diagnosis and treatment of KCNJ11-MODY
by: Juliana Gonçalves, et al.
Published: (2024-12-01)