Skip to main content
NCBI home page
PLOS Genetics logoLink to PLOS Genetics
. 2018 Aug 15;14(8):e1007610. doi: 10.1371/journal.pgen.1007610

Correction: Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy

Caroline Choquet, Thi Hong Minh Nguyen, Pierre Sicard, Emeline Buttigieg, Thi Thom Tran, Frank Kober, Isabelle Varlet, Rachel Sturny, Mauro W Costa, Richard P Harvey, Catherine Nguyen, Pascal Rihet, Sylvain Richard, Monique Bernard, Robert G Kelly, Nathalie Lalevée, Lucile Miquerol
PMCID: PMC6093597  PMID: 30110325

The following information is missing from the Funding section: This study was supported by GRRC (https://sfcardio.fr/grrc/sommaire) to CC.

Reference

  • 1.Choquet C, Nguyen THM, Sicard P, Buttigieg E, Tran TT, Kober F, et al. (2018) Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy. PLoS Genet 14(7): e1007502 10.1371/journal.pgen.1007502 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from PLoS Genetics are provided here courtesy of PLOS

RESOURCES