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