KCNJ2 mutations in arrhythmia patients referred for LQT testing: A mutation T305A with novel effect on rectification properties-Reference-Cited by-同舟云学术

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KCNJ2 mutations in arrhythmia patients referred for LQT testing: A mutation T305A with novel effect on rectification properties

Published:2007-03 Issue:3 Volume:4 Page:323-329
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Eckhardt Lee L.,Farley Amanda L.,Rodriguez Esther,Ruwaldt Karen,Hammill Daniel,Tester David J.,Ackerman Michael J.,Makielski Jonathan C.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen’s syndrome;Plaster;Cell,2001

2. Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies;Andersen;Acta Paediatr Scand,1971

3. Andersen’s syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features;Tawil;Ann Neurol,1994

4. Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype;Zhang;Circulation,2005

5. KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes;Andelfinger;Am J Hum Genet,2002

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4. Inward rectifier potassium (Kir) channels in the retina: living our vision;American Journal of Physiology-Cell Physiology;2022-09-01

5. Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome;European Journal of Neurology;2022-05-04

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