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<mods:namePart>Rivière, Jacques G.</mods:namePart>
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<mods:namePart>Soler-Palacín, Pere</mods:namePart>
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<mods:namePart>Pujol, Aurora</mods:namePart>
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<mods:namePart>Esteller, Manel</mods:namePart>
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<mods:dateAccessioned encoding="iso8601">2025-01-24T11:49:47Z</mods:dateAccessioned>
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<mods:identifier type="issn">2589-5370</mods:identifier>
<mods:identifier type="uri">http://hdl.handle.net/10259/10037</mods:identifier>
<mods:identifier type="doi">10.1016/J.ECLINM.2022.101515</mods:identifier>
<mods:abstract>Most children and adolescents infected with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remain asymptomatic or develop a mild coronavirus disease 2019 (COVID-19) that usually does not require medical intervention. However, a small proportion of pediatric patients develop a severe clinical condition, multisystem inflammatory syndrome in children (MIS-C). The involvement of epigenetics in the control of the immune response and viral activity prompted us to carry out an epigenomic study to uncover target loci regulated by DNA methylation that could be altered upon the appearance of MIS-C.</mods:abstract>
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<mods:accessCondition type="useAndReproduction">Atribución 4.0 Internacional</mods:accessCondition>
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<mods:topic>Multisystem inflammatory syndrome in children</mods:topic>
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<mods:topic>COVID-19</mods:topic>
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<mods:subject>
<mods:topic>Kawasaki disease</mods:topic>
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<mods:topic>Epigenetics</mods:topic>
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<mods:topic>DNA methylation</mods:topic>
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<mods:title>Epigenetic profiling linked to multisystem inflammatory syndrome in children (MIS-C): A multicenter, retrospective study</mods:title>
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