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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

This article is an erratum on:

  1. Case Report: Novel Biallelic Variants in DNAJC21 Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis

    1. Read original article
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An Erratum On
Novel Biallelic Variants in DNAJC21 Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis

by Chirita-Emandi, A., Petrescu, C.-A.-M., Zimbru, C. G., Stoica, F., Marian, C., Ciubotaru, A., Bataneant M. and Puiu M. (2022). Front. Genet. 10:870233. doi: 10.3389/fgene.2022.870233

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.

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.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

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