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First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy

Janin, Alexandre et al.

Gene. Volume 676: (2018, November 15th); pp 110-116

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TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome

Janin, Alexandre et al.

European journal of medical genetics. Volume 62:Number 6 (2019, June) -- Elsevier

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Blockade of the renin‐angiotensin‐aldosterone system in patients with arrhythmogenic right ventricular dysplasia: A double‐blind, multicenter, prospective, randomized, genotype‐driven study (BRAVE study)

Morel, Elodie et al.

Clinical cardiology. Volume 41:Issue 3 (2018); pp 300-306 -- Wiley

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