KVLQT1 mutations in three families with familial or sporadic long QT syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/5/9/1319/1663207/5-9-1319.pdf
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1. Targeted deep sequencing analyses of long QT syndrome in a Japanese population;PLOS ONE;2022-12-08
2. Kv Channel Ancillary Subunits: Where Do We Go from Here?;Physiology;2022-09-01
3. Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation;Scientific Reports;2021-02-11
4. Physiological Functions, Biophysical Properties, and Regulation of KCNQ1 (KV7.1) Potassium Channels;Ion Channels in Biophysics and Physiology;2021
5. Deconstruction of an African folk medicine uncovers a novel molecular strategy for therapeutic potassium channel activation;Science Advances;2018-11-02
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