Front. Neurol. Frontiers in Neurology Front. Neurol. 1664-2295 Frontiers Media S.A. 10.3389/fneur.2019.00936 Neurology Correction Addendum: A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene Li Tao-Ran 1 2 Wang Qun 1 Liu Mao-Mao 1 Lv Rui-Juan 1 * 1Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, China 2Department of Neurology, XuanWu Hospital of Capital Medical University, Beijing, China

Edited and reviewed by: Christos Proukakis, University College London, United Kingdom

 *Correspondence: Rui-Juan Lv lvruijuan1981@126.com

This article was submitted to Neurogenetics, a section of the journal Frontiers in Neurology

 18 09 2019 2019 10 936 31 05 2019 12 08 2019 Copyright © 2019 Li, Wang, Liu and Lv. 2019 Li, Wang, Liu and Lv

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 An Addendum on A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene by Li, T.-R., Wang, Q., Liu, M.-M., and Lv, R.-J. (2019). Front. Neurol. 10:347. doi: 10.3389/fneur.2019.00347 Leigh syndrome Leigh-like syndrome MELAS MELAS-LS overlap syndrome m.10191T>C mutation

In the original article, there was an error. There were two spelling mistakes in the article.

A correction has been made to Discussion and Conclusion, last sentence of Paragraph 8:

“Recognition of the characteristics of these patients with the T10191C mutation will help us improve the clinical understanding of LS or Leigh-like syndrome.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Addendum

In the original article, we had not obtained the heteroplasmy levels of the proband and her aunt from the gene sequencing company at the time of manuscript publication.

Through follow-up research, we make the following addendum:

By detecting the proband's and her aunt's blood sample, we found the heteroplasmy level of the proband is 33.2% (forward percent) or 38.2% (reverse percent) respectively, the heteroplasmy level of her aunt is 4.4% (forward percent) or 4.8% (reverse percent), respectively.