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Exposome-wide Association Study for Metabolic Syndrome

Detalles Bibliográficos
Autores principales: Gao, Peng, Snyder, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688998/
https://www.ncbi.nlm.nih.gov/pubmed/34950191
http://dx.doi.org/10.3389/fgene.2021.783930
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author Gao, Peng
Snyder, Michael
author_facet Gao, Peng
Snyder, Michael
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spelling pubmed-86889982021-12-22 Exposome-wide Association Study for Metabolic Syndrome Gao, Peng Snyder, Michael Front Genet Genetics Frontiers Media S.A. 2021-12-07 /pmc/articles/PMC8688998/ /pubmed/34950191 http://dx.doi.org/10.3389/fgene.2021.783930 Text en Copyright © 2021 Gao and Snyder. https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Genetics
Gao, Peng
Snyder, Michael
Exposome-wide Association Study for Metabolic Syndrome
title Exposome-wide Association Study for Metabolic Syndrome
title_full Exposome-wide Association Study for Metabolic Syndrome
title_fullStr Exposome-wide Association Study for Metabolic Syndrome
title_full_unstemmed Exposome-wide Association Study for Metabolic Syndrome
title_short Exposome-wide Association Study for Metabolic Syndrome
title_sort exposome-wide association study for metabolic syndrome
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688998/
https://www.ncbi.nlm.nih.gov/pubmed/34950191
http://dx.doi.org/10.3389/fgene.2021.783930
work_keys_str_mv AT gaopeng exposomewideassociationstudyformetabolicsyndrome
AT snydermichael exposomewideassociationstudyformetabolicsyndrome