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

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Title: Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence.
Authors: Zinchenko RA; Research Centre for Medical Genetics, Moscow, Russia.; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia., Ginter EK; Research Centre for Medical Genetics, Moscow, Russia., Marakhonov AV; Research Centre for Medical Genetics, Moscow, Russia., Petrova NV; Research Centre for Medical Genetics, Moscow, Russia., Kadyshev VV; Research Centre for Medical Genetics, Moscow, Russia., Vasilyeva TP; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia., Alexandrova OU; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia., Polyakov AV; Research Centre for Medical Genetics, Moscow, Russia., Kutsev SI; Research Centre for Medical Genetics, Moscow, Russia.
Source: Frontiers in genetics [Front Genet] 2022 Sep 09; Vol. 13, pp. 1019916. Date of Electronic Publication: 2022 Sep 09 (Print Publication: 2022).
Publication Type: Published Erratum
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence.
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  Data: <searchLink fieldCode="AU" term="%22Zinchenko+RA%22">Zinchenko RA</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Ginter+EK%22">Ginter EK</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Marakhonov+AV%22">Marakhonov AV</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Petrova+NV%22">Petrova NV</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Kadyshev+VV%22">Kadyshev VV</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Vasilyeva+TP%22">Vasilyeva TP</searchLink>; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Alexandrova+OU%22">Alexandrova OU</searchLink>; Department of Public Health Research, N.A. Semashko National Research Institute of Public Health, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Polyakov+AV%22">Polyakov AV</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.<br /><searchLink fieldCode="AU" term="%22Kutsev+SI%22">Kutsev SI</searchLink>; Research Centre for Medical Genetics, Moscow, Russia.
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  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2022 Sep 09; Vol. 13, pp. 1019916. <i>Date of Electronic Publication: </i>2022 Sep 09 (<i>Print Publication: </i>2022).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.3389/fgene.2022.1019916
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        Text: English
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            – D: 09
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              Text: 2022 Sep 09
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