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Correction to: Comprehensive genetic characteristics of dystrophinopathies in China
Orphanet Journal of Rare Diseases volume 16, Article number: 252 (2021)
The Original Article was published on 04 July 2018
Correction to: Ma et al. Orphanet Journal of Rare Diseases https://doi.org/10.1186/s13023-018-0853-z
The authors are grateful to the Editor of Orphanet Journal of Rare Diseases for allowing them the opportunity to publish this Correction, and apologize to the readership for any inconvenience caused.
A number of the variant descriptions in Additional file 1 of the original article [1] were not correct because of using different Refseq. The authors have now revised all the variant descriptions by Reference Sequence Database (NM_004006.2) in “Additional file 1” accompanying this Correction, as well as the original article.
All the authors agree to this Correction.
Reference
Ma, et al. Comprehensive genetic characteristics of dystrophinopathies in China. Orphanet J Rare Dis. 2018;13:109. https://doi.org/10.1186/s13023-018-0853-z.
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Supplementary Information
Additional file 1
. Clinical and genetic information of patients with small mutation.
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Ma, P., Zhang, S., Zhang, H. et al. Correction to: Comprehensive genetic characteristics of dystrophinopathies in China. Orphanet J Rare Dis 16, 252 (2021). https://doi.org/10.1186/s13023-021-01853-x
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DOI: https://doi.org/10.1186/s13023-021-01853-x