Correction: De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies
Nirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, Sadhana Gaddam, Casey Gifford, Jamal Nasir, Ioannis Karakikes
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsCardiomyopathy and Myosin Studies · Congenital heart defects research · Neurogenetic and Muscular Disorders Research
Correction: Human Genomics (2022) 16:55 10.1186/s40246-022-00420-0
The article has been updated to remove identifying information.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Vadgama N, Ameen M, Sundaram L, Gaddam S, Genomics England Research Consortium, Gifford C, Nasir J, Karakikes I. De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies. Hum Genom. 2022; 16:55. 10.1186/s 40246-022-00420-0.10.1186/s 40246-022-00420-0PMC 964798336357925 · doi ↗ · pubmed ↗