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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2021 Jun 1;16:247. doi: 10.1186/s13023-021-01892-4

Correction to: Molecular mechanics and dynamic simulations of well-known Kabuki syndrome-associated KDM6A variants reveal putative mechanisms of dysfunction

Young-In Chi 1,2,3, Timothy J Stodola 1,2, Thiago M De Assuncao 1,3, Elise N Levrence 1, Swarnendu Tripathi 1,2, Nikita R Dsouza 1,2, Angela J Mathison 1,2,3, Donald G Basel 1,4, Brian F Volkman 5, Brian C Smith 5, Gwen Lomberk 1,3,6, Michael T Zimmermann 1,2,7, Raul Urrutia 1,2,3,4,
PMCID: PMC8170813  PMID: 34074320

Correction to: Orphanet J Rare Dis (2021) 16:66 10.1186/s13023-021-01692-w

After the publication of the original article [1], the authors became aware of the work by Petrizzelli et al., 2020 [2]. The two studies truly represent independent works, for which contents are different. Indeed, although both studies contain molecular dynamics data, each of them use different approaches as well as derived sets of analysis and interpretations which are different in depth of information. Therefore, both studies should be considered complementary to each other.

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References

  • 1.Chi, et al. Molecular mechanics and dynamic simulations of well-known Kabuki syndrome-associated KDM6A variants reveal putative mechanisms of dysfunction. Orphanet J Rare Dis. 2021;16:66. doi: 10.1186/s13023-021-01692-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Petrizzelli, et al. Mechanisms of pathogenesis of missense mutations on the KDM6A-H3 interaction in type 2 Kabuki syndrome. Comput Struct Biotechnol J. 2020;18:2033–2042. doi: 10.1016/j.csbj.2020.07.013. [DOI] [PMC free article] [PubMed] [Google Scholar]

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