Rare disease informs mechanism and possible treatment of statin-associated myopathy

Detalles Bibliográficos
Autor principal: Harel, Tamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013738/
https://www.ncbi.nlm.nih.gov/pubmed/36848568
http://dx.doi.org/10.1073/pnas.2300988120
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author Harel, Tamar
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spelling pubmed-100137382023-08-27 Rare disease informs mechanism and possible treatment of statin-associated myopathy Harel, Tamar Proc Natl Acad Sci U S A Commentary National Academy of Sciences 2023-02-27 2023-03-07 /pmc/articles/PMC10013738/ /pubmed/36848568 http://dx.doi.org/10.1073/pnas.2300988120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Commentary
Harel, Tamar
Rare disease informs mechanism and possible treatment of statin-associated myopathy
title Rare disease informs mechanism and possible treatment of statin-associated myopathy
title_full Rare disease informs mechanism and possible treatment of statin-associated myopathy
title_fullStr Rare disease informs mechanism and possible treatment of statin-associated myopathy
title_full_unstemmed Rare disease informs mechanism and possible treatment of statin-associated myopathy
title_short Rare disease informs mechanism and possible treatment of statin-associated myopathy
title_sort rare disease informs mechanism and possible treatment of statin-associated myopathy
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013738/
https://www.ncbi.nlm.nih.gov/pubmed/36848568
http://dx.doi.org/10.1073/pnas.2300988120
work_keys_str_mv AT hareltamar rarediseaseinformsmechanismandpossibletreatmentofstatinassociatedmyopathy