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You searched for: Author/Creator Stallmeyer, Birgit

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1. Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy. (August 2019)

2. Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort. (August 2019)

3. Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography. Issue 4 (1st September 2017)

4. Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death. (15th April 2021)

5. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Issue 4 (28th July 2020)

6. POPDC2 a novel susceptibility gene for conduction disorders. (August 2020)

7. Sodium permeable and "hypersensitive" TREK‐1 channels cause ventricular tachycardia. Issue 4 (27th February 2017)

8. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. (March 2015)

9. A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction. Issue 10 (12th May 2017)

10. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. (March 2015)