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. 2012 Jul 19;20(8):910. doi: 10.1038/ejhg.2012.123

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Helen AL Tuppen, Karin Naess, Nancy G Kennaway, Mazhor Al-Dosary, Nicole Lesko, John W Yarham, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Richard G Weleber, Emma L Blakely, Robert W Taylor, Robert McFarland
PMCID: PMC3400725

Correction to: European Journal of Human Genetics (2012) 20, 897–904; doi:10.1038/ejhg.2012.44

Since the publication of this article, the authors have noticed that they had omitted funding information, and that the Figure 2 legend needed clarification. These issues have now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified.

The authors would like to apologise for their oversight.

Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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