Corrigendum: spondyloocular syndrome: a novel xylt2 variant with description of the neonatal phenotype

HIGHLIGHTS

• who: Correction and collaborators from the Frontiers Media SA, SwitzerlandMedical Genetics, University of Siena, Siena, Tuscany, Italy, Med Biotech Hub and Competence Center have published the research: Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype, in the Journal: (JOURNAL)

SUMMARY

Spondyloocular syndrome (SOS), xylosyltransferase II, Exome Sequencing (ES), skeletal dysplasia, XYLT2 COPYRIGHT A Corrigendum on Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype by Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, Coradeschi C, Grosso S, Tomasini B, Mencarelli MA . . .

 



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