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Editorial: Whole Genome Sequencing for rare diseases

Detalles Bibliográficos
Autores principales: Di Resta, Chiara, D'Argenio, Valeria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546400/
https://www.ncbi.nlm.nih.gov/pubmed/37795418
http://dx.doi.org/10.3389/fmed.2023.1267930
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author Di Resta, Chiara
D'Argenio, Valeria
author_facet Di Resta, Chiara
D'Argenio, Valeria
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spelling pubmed-105464002023-10-04 Editorial: Whole Genome Sequencing for rare diseases Di Resta, Chiara D'Argenio, Valeria Front Med (Lausanne) Medicine Frontiers Media S.A. 2023-09-19 /pmc/articles/PMC10546400/ /pubmed/37795418 http://dx.doi.org/10.3389/fmed.2023.1267930 Text en Copyright © 2023 Di Resta and D'Argenio. 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 Medicine
Di Resta, Chiara
D'Argenio, Valeria
Editorial: Whole Genome Sequencing for rare diseases
title Editorial: Whole Genome Sequencing for rare diseases
title_full Editorial: Whole Genome Sequencing for rare diseases
title_fullStr Editorial: Whole Genome Sequencing for rare diseases
title_full_unstemmed Editorial: Whole Genome Sequencing for rare diseases
title_short Editorial: Whole Genome Sequencing for rare diseases
title_sort editorial: whole genome sequencing for rare diseases
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546400/
https://www.ncbi.nlm.nih.gov/pubmed/37795418
http://dx.doi.org/10.3389/fmed.2023.1267930
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