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The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy

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Description scientific article published on 22 May 2019
Author/s

author: Nicolò Salvarani  Gianfranco Sinagra  Charles Murry  Alessandro Bertero  Michele Miragoli  Marianna Paulis  Gianluigi Condorelli  Paolo Kunderfranco 

Publication date May 22, 2019
Language English
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