Search

Search Constraints

You searched for: Author/Creator Schott, Jean‐Jacques

Search Results

1. A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype. Issue 6 (6th June 2021)

2. Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management. Issue 9 (23rd July 2022)

3. Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome. Issue 6 (10th June 2016)

4. Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome. Issue 6 (June 2016)

5. DZIP1 regulates mammalian cardiac valve development through a Cby1‐β‐catenin mechanism. Issue 10 (9th April 2021)

6. EDiVA—Classification and prioritization of pathogenic variants for clinical diagnostics. Issue 7 (21st May 2019)

7. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes. Issue 9 (13th September 2016)

8. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes. Issue 9 (September 2016)

9. Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block. Issue 5 (20th May 2016)

10. Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block. Issue 5 (May 2016)