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. 2016 Dec 1;99(6):1405. doi: 10.1016/j.ajhg.2016.11.001

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Kyle Thompson, Homa Majd, Cristina Dallabona, Karit Reinson, Martin S King, Charlotte L Alston, Langping He, Tiziana Lodi, Simon A Jones, Aviva Fattal-Valevski, Nitay D Fraenkel, Ann Saada, Alon Haham, Pirjo Isohanni, Roshni Vara, Inês A Barbosa, Michael A Simpson, Charu Deshpande, Sanna Puusepp, Penelope E Bonnen, Richard J Rodenburg, Anu Suomalainen, Katrin Õunap, Orly Elpeleg, Ileana Ferrero, Robert McFarland, Edmund RS Kunji, Robert W Taylor ∗
PMCID: PMC5142113  PMID: 27912046

(The American Journal of Human Genetics 99, 860–876; October 6, 2016)

In the originally published version of this article, Cristina Dallabona’s first name was unfortunately misspelled. It appears correctly here and online. The authors regret the error.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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