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ERRATUM article

Front. Neurol., 20 September 2023
Sec. Neurogenetics
Volume 14 - 2023 | https://doi.org/10.3389/fneur.2023.1290996
This article is part of the Research Topic Consanguinity and Rare Genetic Neurological Diseases View all 8 articles

Erratum: Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane

This article is an erratum on:

  1. Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane

    1. Read original article
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An Erratum on
Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane

by Xu, H., Lv, H., Chen, X., Lian, Y., Xing, G., Wang, Y., and Hu, R. (2023). Front. Neurol. 14:1231605. doi: 10.3389/fneur.2023.1231605

Due to a production error, a correction has been made to the Data Availability Statement. The paragraph now reads:

“The original contributions presented in the study are publicly available. This data can be found here: European Molecular Biology Laboratory's European Bioinformatics Institute (EMBL-EBI), European Variation Archive (EVA), https://www.ebi.ac.uk/eva/, PRJEB65581.”

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

Keywords: Wilson's disease, ATP7B gene, novel mutations, renal pathological, liver transplantation

Citation: Frontiers Production Office (2023) Erratum: Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane. Front. Neurol. 14:1290996. doi: 10.3389/fneur.2023.1290996

Received: 08 September 2023; Accepted: 08 September 2023;
Published: 20 September 2023.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

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