Prevalence and cardiometabolic correlates of ketohexokinase gene variants among UK Biobank participants

Essential fructosuria (EF) is a benign, asymptomatic, autosomal recessive condition caused by loss-of-function variants in the ketohexokinase gene and characterized by intermittent appearance of fructose in the urine. Despite a basic understanding of the genetic and molecular basis of EF, relatively...

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Detalles Bibliográficos
Autores principales: Johnston, Joseph A., Nelson, David R., Bhatnagar, Pallav, Curtis, Sarah E., Chen, Yu, MacKrell, James G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901775/
https://www.ncbi.nlm.nih.gov/pubmed/33621267
http://dx.doi.org/10.1371/journal.pone.0247683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901775/
https://www.ncbi.nlm.nih.gov/pubmed/33621267
http://dx.doi.org/10.1371/journal.pone.0247683

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