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CORRECTION article

Front. Genet., 09 September 2022
Sec. Evolutionary and Population Genetics
Volume 13 - 2022 | https://doi.org/10.3389/fgene.2022.1019916
This article is part of the Research Topic Association Between Individuals’ Genomic Ancestry and Variation in Disease Susceptibility View all 13 articles

Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence

This article is a correction to:

  1. Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative Prevalence

    1. Read original article
Rena A. Zinchenko, Rena A. Zinchenko1,2*Eugeny K. GinterEugeny K. Ginter1Andrey V. Marakhonov Andrey V. Marakhonov1*Nika V. PetrovaNika V. Petrova1Vitaly V. KadyshevVitaly V. Kadyshev1Tatyana P. VasilyevaTatyana P. Vasilyeva2Oksana U. AlexandrovaOksana U. Alexandrova2Alexander V. PolyakovAlexander V. Polyakov1Sergey I. KutsevSergey I. Kutsev1
  • 1Research Centre for Medical Genetics, Moscow, Russia
  • 2Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia

A Corrigendum on
Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence

by Zinchenko RA, Ginter EK, Marakhonov AV, Petrova NV, Kadyshev VV, Vasilyeva TP, Alexandrova OU, Polyakov AV and Kutsev SI (2021). Front. Genet. 12:678957. doi: 10.3389/fgene.2021.678957

In the published article, there was an error in the Funding statement. The state assignment of the Ministry of Science and Higher Education of the Russian Federation was incorrectly mentioned as a funding source. The correct Funding statement appears below:

“This study was supported by the Russian Science Foundation, grant no. 17-15-01051.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s note

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.

Keywords: genetic epidemiology, rare hereditary diseases, point prevalence, cumulative prevalence, Russia

Citation: Zinchenko RA, Ginter EK, Marakhonov AV, Petrova NV, Kadyshev VV, Vasilyeva TP, Alexandrova OU, Polyakov AV and Kutsev SI (2022) Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence. Front. Genet. 13:1019916. doi: 10.3389/fgene.2022.1019916

Received: 15 August 2022; Accepted: 18 August 2022;
Published: 09 September 2022.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2022 Zinchenko, Ginter, Marakhonov, Petrova, Kadyshev, Vasilyeva, Alexandrova, Polyakov and Kutsev. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Rena A. Zinchenko, renazinchenko@mail.ru; Andrey V. Marakhonov, marakhonov@generesearch.ru

Disclaimer: 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.