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

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

Bibliographic Details
Main Authors:	Gabriella Doddato, Alessandra Fabbiani, Chiara Fallerini, Mirella Bruttini, Theodora Hadjistilianou, Martino Landi, Caterina Coradeschi, Salvatore Grosso, Barbara Tomasini, Maria Antonietta Mencarelli, Alessandra Renieri, Francesca Ariani
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2023-01-01
Series:	Frontiers in Genetics
Subjects:	spondyloocular syndrome (SOS) xylosyltransferase II Exome Sequencing (ES) skeletal dysplasia XYLT2
Online Access:	https://www.frontiersin.org/articles/10.3389/fgene.2023.1143795/full

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