Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies
Author:
Affiliation:
1. R.N.E Laboratory, Multidisciplinary Faculty of Taza, University of Sidi Mohamed Ben Abdellah, Fez, Morocco
2. Department of Biology and Earth Sciences, Regional Center for Education Careers and Training, Fez, Morocco
Abstract
Publisher
Hindawi Limited
Subject
Pharmacology (medical),Cardiology and Cardiovascular Medicine,Pharmacology,General Medicine
Link
http://downloads.hindawi.com/journals/cdtp/2020/6615038.pdf
Reference83 articles.
1. Structure of the human TRPM4 ion channel in a lipid nanodisc
2. Structure of full-length human TRPM4
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4. Glycosylation of TRPM4 and TRPM5 channels: molecular determinants and functional aspects
5. Electron cryo-microscopy structure of a human TRPM4 channel
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