ERRATUM article

Front. Genet., 25 May 2022

Sec. Genetics of Common and Rare Diseases

Volume 13 - 2022 | https://doi.org/10.3389/fgene.2022.930132

Erratum: Novel Biallelic Variants in DNAJC21 Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis

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    Frontiers Production Office *

  • Frontiers Media SA, Lausanne, Switzerland

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Due to a production error, there was an error in author Affiliations 2 and 6.

A correction has been added to Acknowledgements, “The Regional Center of Medical Genetics Timis, Clinical Emergency Hospital for Children “Louis Turcanu” Timisoara, Timis, Romania is part of European Reference Network ERN ITHACA. The Department of Ophthalmology, Municipal Clinical Emergency Hospital of Timisoara, Timisoara, Romania is part of European Reference Network ERN-EYE.”

The publisher apologizes for this mistake. The original version of this article has been updated.

Summary

Keywords

DNAJC21 gene, ribosomopathy, bone marrow failure syndrome, Shwachman–Diamond syndrome, telomeres

Citation

Frontiers Production Office (2022) Erratum: Novel Biallelic Variants in DNAJC21 Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis. Front. Genet. 13:930132. doi: 10.3389/fgene.2022.930132

Received

27 April 2022

Accepted

27 April 2022

Published

25 May 2022

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Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

13 - 2022

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Copyright

*Correspondence: Frontiers Production Office,

This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Genetics

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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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