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MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes.
Lee, Yee-Ki; Sala, Luca; Mura, Manuela; Rocchetti, Marcella; Pedrazzini, Matteo; Ran, Xinru; Mak, Timothy S H; Crotti, Lia; Sham, Pak C; Torre, Eleonora; Zaza, Antonio; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano.
Afiliación
  • Lee YK; Cardiology Division, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Sala L; Hong Kong-Guangdong Joint Laboratory on Stem Cell and Regenerative Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Mura M; Department of Biotechnologies and Biosciences, University of Milano-Bicocca, Milano, Italy.
  • Rocchetti M; Istituto Auxologico Italiano, IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy.
  • Pedrazzini M; Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Ran X; Department of Cardiothoracic and Vascular Sciences, Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Mak TSH; Department of Biotechnologies and Biosciences, University of Milano-Bicocca, Milano, Italy.
  • Crotti L; Istituto Auxologico Italiano, IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy.
  • Sham PC; Cardiology Division, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Torre E; Hong Kong-Guangdong Joint Laboratory on Stem Cell and Regenerative Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Zaza A; Guangzhou Institutes of Biomedicine and Health, Guangzhou, China.
  • Schwartz PJ; Department of Psychiatry, The University of Hong Kong, Hong Kong SAR, China.
  • Tse HF; Istituto Auxologico Italiano, IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Milan, Italy.
  • Gnecchi M; Department of Cardiovascular, Neural and Metabolic Sciences, Istituto Auxologico Italiano, IRCCS, San Luca Hospital, Milan, Italy.
Cardiovasc Res ; 117(3): 767-779, 2021 02 22.
Article en En | MEDLINE | ID: mdl-32173736
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Polimorfismo de Nucleótido Simple / Canal de Potasio KCNQ1 / Proteínas Tirosina Fosfatasas no Receptoras / Genes Modificadores / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cardiovasc Res Año: 2021 Tipo del documento: Article País de afiliación: China
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Polimorfismo de Nucleótido Simple / Canal de Potasio KCNQ1 / Proteínas Tirosina Fosfatasas no Receptoras / Genes Modificadores / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cardiovasc Res Año: 2021 Tipo del documento: Article País de afiliación: China