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

MLA

Doddato, Gabriella, et al. “Corrigendum: Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype.” Frontiers in Genetics, vol. 14, Jan. 2023, p. 1143795. EBSCOhost, https://doi.org/10.3389/fgene.2023.1143795.

APA

Doddato, G., Fabbiani, A., Fallerini, C., Bruttini, M., Hadjistilianou, T., Landi, M., Coradeschi, C., Grosso, S., Tomasini, B., Mencarelli, M. A., Renieri, A., & Ariani, F. (2023). Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype. Frontiers in Genetics, 14, 1143795. https://doi.org/10.3389/fgene.2023.1143795

Chicago

Doddato, Gabriella, Alessandra Fabbiani, Chiara Fallerini, Mirella Bruttini, Theodora Hadjistilianou, Martino Landi, Caterina Coradeschi, et al. 2023. “Corrigendum: Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype.” Frontiers in Genetics 14 (January): 1143795. doi:10.3389/fgene.2023.1143795.