Nexilin mutations are associated with left ventricular noncompaction cardiomyopathy
2015 · Molecular and Cellular Pediatrics · 12 citations
https://doi.org/10.1186/2194-7791-2-s1-a7
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HH Krämer is an academic researcher. The author has contributed to research in topics: Congenital Heart Disease Studies & Cardiovascular Function and Risk Factors & Congenital heart defects research. The author has an h-index of 6, co-authored 29 publications.
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