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Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905838/ https://www.ncbi.nlm.nih.gov/pubmed/36761000 http://dx.doi.org/10.3389/fgene.2023.1143795 |
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| author | Doddato, Gabriella Fabbiani, Alessandra Fallerini, Chiara Bruttini, Mirella Hadjistilianou, Theodora Landi, Martino Coradeschi, Caterina Grosso, Salvatore Tomasini, Barbara Mencarelli, Maria Antonietta Renieri, Alessandra Ariani, Francesca |
| author_facet | Doddato, Gabriella Fabbiani, Alessandra Fallerini, Chiara Bruttini, Mirella Hadjistilianou, Theodora Landi, Martino Coradeschi, Caterina Grosso, Salvatore Tomasini, Barbara Mencarelli, Maria Antonietta Renieri, Alessandra Ariani, Francesca |
| author_sort | Doddato, Gabriella |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9905838 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Frontiers Media S.A. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-99058382023-02-08 Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype Doddato, Gabriella Fabbiani, Alessandra Fallerini, Chiara Bruttini, Mirella Hadjistilianou, Theodora Landi, Martino Coradeschi, Caterina Grosso, Salvatore Tomasini, Barbara Mencarelli, Maria Antonietta Renieri, Alessandra Ariani, Francesca Front Genet Genetics Frontiers Media S.A. 2023-01-25 /pmc/articles/PMC9905838/ /pubmed/36761000 http://dx.doi.org/10.3389/fgene.2023.1143795 Text en Copyright © 2023 Doddato, Fabbiani, Fallerini, Bruttini, Hadjistilianou, Landi, Coradeschi, Grosso, Tomasini, Mencarelli, Renieri and Ariani. 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 Doddato, Gabriella Fabbiani, Alessandra Fallerini, Chiara Bruttini, Mirella Hadjistilianou, Theodora Landi, Martino Coradeschi, Caterina Grosso, Salvatore Tomasini, Barbara Mencarelli, Maria Antonietta Renieri, Alessandra Ariani, Francesca Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title | Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title_full | Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title_fullStr | Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title_full_unstemmed | Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title_short | Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype |
| title_sort | corrigendum: spondyloocular syndrome: a novel xylt2 variant with description of the neonatal phenotype |
| topic | Genetics |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905838/ https://www.ncbi.nlm.nih.gov/pubmed/36761000 http://dx.doi.org/10.3389/fgene.2023.1143795 |
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