Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
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

Internet

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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