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Your search keyword '"Boven, Ludolf G."' showing total 18 results

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18 results on '"Boven, Ludolf G."'

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1. Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants

2. The effect of tropomyosin variants on cardiomyocyte function and structure that underlie different clinical cardiomyopathy phenotypes

3. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

4. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

5. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

6. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

7. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

8. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

9. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy

10. Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy (Scientific Reports, (2019), 9, 1, (4093), 10.1038/s41598-019-39911-x)

11. No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

12. No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

13. No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

14. No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

15. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

16. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

17. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

18. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

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