ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy.
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Good JM
Department of Genetic Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Fellmann F
Department of Genetic Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Bhuiyan ZA
Department of Genetic Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Rotman S
Service of Clinical Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Pruvot E
Department of Cardiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Schläpfer J
Department of Cardiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
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Published in:
- HeartRhythm case reports. - 2020
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gold
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https://sonar.ch/global/documents/186373
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