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Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces

Detalles Bibliográficos
Autores principales: Valli, Roberto, Penzo, Marianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131078/
https://www.ncbi.nlm.nih.gov/pubmed/37124624
http://dx.doi.org/10.3389/fgene.2023.1194788
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author Valli, Roberto
Penzo, Marianna
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Penzo, Marianna
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spelling pubmed-101310782023-04-27 Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces Valli, Roberto Penzo, Marianna Front Genet Genetics Frontiers Media S.A. 2023-04-12 /pmc/articles/PMC10131078/ /pubmed/37124624 http://dx.doi.org/10.3389/fgene.2023.1194788 Text en Copyright © 2023 Valli and Penzo. 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
Valli, Roberto
Penzo, Marianna
Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title_full Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title_fullStr Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title_full_unstemmed Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title_short Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces
title_sort editorial: inherited and acquired ribosomopathies: missing puzzle pieces
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131078/
https://www.ncbi.nlm.nih.gov/pubmed/37124624
http://dx.doi.org/10.3389/fgene.2023.1194788
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