Correction to: European Journal of Human Genetics (2015) 23, 325–330; doi:10.1038/ejhg.2014.128
The sub-heading of Table 1 is incorrect and should read:
Additional information
The online version of the original article can be found at 10.1038/ejhg.2014.128
Rights and permissions
About this article
Cite this article
Matilainen, S., Isohanni, P., Euro, L. et al. Erratum: Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion. Eur J Hum Genet 25, 393–0 (2017). https://doi.org/10.1038/ejhg.2016.166
Published:
Issue Date:
DOI: https://doi.org/10.1038/ejhg.2016.166
