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Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8
Orphanet Journal of Rare Diseases volume 16, Article number: 505 (2021)
The Original Article was published on 20 September 2021
Correction to: Orphanet J Rare Dis (2021) 16:392 https://doi.org/10.1186/s13023-021-02018-6
Following the publication of the original article [1] the authors asked to revise the following sentence of the “Discussion” section:
"Another special IBDD patient, with a severe lack of speech development and lack of social interactions, was reported to be associated with autism that was genetically confirmed in the DNA2 gene [18]."
The correct sentence should read:
"Another special IBDD patient, with a severe lack of speech development and lack of social interactions, was reported to be associated with autism [18]."
The original article has already been corrected as above.
Reference
Feng J, et al. Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8. Orphanet J Rare Dis. 2021;16:392. https://doi.org/10.1186/s13023-021-02018-6.
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Feng, J., Yang, C., Zhu, L. et al. Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8. Orphanet J Rare Dis 16, 505 (2021). https://doi.org/10.1186/s13023-021-02132-5
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DOI: https://doi.org/10.1186/s13023-021-02132-5